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  • 1985-1989  (30)
  • 1960-1964  (10)
  • 1920-1924
  • 1910-1914
  • 1900-1904
  • Synthetic methods
  • 1
    ISSN: 0570-0833
    Schlagwort(e): Metallo-ene reaction ; Ene reaction ; Synthetic methods ; Catalysis ; Natural products ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Metallo-ene reactions, hardly recognized until very recently, have experienced a breathtaking development when applied in an intramolecular sense. Efficient regio- and stereoselective magnesium-ene cyclizations have served as a cornerstone for numerous syntheses of structurally diverse natural products (e.g., sesquiterpenes of marine or plant origin, alkaloids, fragrances, insect defense compounds, and a fungitoxin). A brilliant example is the synthesis of the elusive odorant (+)-khusimone which outshines 20 years of work in the field of tricyclovetivane synthesis. Palladium-, platinum-, and nickel-catalyzed versions of the metallo-ene reaction are in a comparatively early stage of exploration, but, nevertheless, reveal intriguing potential. Hence an almost 100% stereospecific C—O→C—;Pd-→ C—C chirality transfer permits simple and selective, cis- or trans-annelation processes. The mild cyclization conditions are compatible with various functional groups, such as nitrogen moieties, which offer interesting perspectives for the preparation of heterocycles (e.g., alkaloids) difficult to obtain by other methods. Carbon monoxide insertion reactions of the cyclized σ-metal intermediates were shown to afford annelated cyclopentanones and cyclopentenones with concomitant stereocontrolled formation of four carbon-carbon bonds. These and other observations, highlighted in this article, provide a platform for further extensions and applications of this powerful method in organic synthesis.
    Zusätzliches Material: 11 Tab.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 28 (1989), S. 716-734 
    ISSN: 0570-0833
    Schlagwort(e): Gene technology ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Oligonucleotide synthesis, until a few years ago the rather exotic preserve of a few experts, has become an integral part of the arsenal of molecular-biological techniques. The last decade, in particular, has seen unbelievably rapid development in this area. DNA synthesis has been automated and can now produce genes greater than 1000 base pairs in length. Tailor-made synthetic genes also permit the synthesis of altered or even novel proteins (de novo protein design) by gene-technological methods. Together with modern methods of gene isolation, sequencing, and expression, gene synthesis has played a major part in the enormous advances achieved in gene technology.
    Zusätzliches Material: 12 Ill.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 28 (1989), S. 1173-1192 
    ISSN: 0570-0833
    Schlagwort(e): Cyclization ; Allylic alkylation ; Alkylation ; Synthetic methods ; Palladium ; Catalysis ; C-C coupling ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The history of ring systems in organic chemistry parallels their synthetic accessibility. Transition-metal-catalyzed cyclizations offer a new opportunity to create carbo- and heterocyclic compounds with great facility. Among these methods, allylic alkylations catalyzed by palladium have proven unusually productive because of the extraordinary chemo-, regio-, and diastereoselectivity and the continuing possibility for the development of enantioselectivity. The rules for ring closure differ from those for non-transition-metal-catalyzed reactions. A major benefit is the ability to generate medium (eight-, nine-, ten-, and eleven-membered) and large rings in preference to normal (five-, six- and seven-membered) rings. With the appropriate substrate, efficient macrocyclizations are possible under conditions of normal concentrations. A second major benefit derives from the complementary stereochemistry of the metalcatalyzed substitution (net retention of configuration) compared to non-metal-catalyzed reactions (inversion of configuration). Further, the requirement for the substrate to conform to the transition-metal template may impose a stereochemical preference in the intermediate that ultimately translates into the thermodynamically less stable organic product regardless of the stereochemistry of the starting material. While more work has focused on carbocyclic synthesis, the possibilities for heterocyclic synthesis are just beginning to be tapped. In addition to forming heterocycles by C—C bond formation, use of a heteroatom as a nucleophile has already proven effective for oxygen and nitrogen, with other nucleophiles awaiting investigation. New dimensions for cyclization via allylic alkylation arise by generating the requisite π-allylpalladium intermediates by methods other than palladium(0)-initiated allylic ionizations. In addition, metals other than palladium will clearly expand the possibilities, but as yet remain untapped.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 28 (1989), S. 695-707 
    ISSN: 0570-0833
    Schlagwort(e): Enantioselectivity ; Lipases ; Synthetic methods ; Enzyme catalysis ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Enantioselective biocatalysis in nonaqueous media is becoming increasingly important in preparative synthetic chemistry. This article discusses (1) the general catalytic properties of enzymes in nonaqueous environments, (2) the basic principles that govern lipase-catalyzed enantioselective esterification and transesterification reactions in organic media for the preparation of optically active acids and alcohols, (3) the determination of kinetic and thermodynamic parameters, and (4) the quantitative analysis of published data.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 28 (1989), S. 969-980 
    ISSN: 0570-0833
    Schlagwort(e): Stereoselectivity ; Reaction mechanisms ; Synthetic methods ; Free radicals ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The regio- and chemoselectivities of free radical reactions are often high and largely predictable; systematic studies have now shown that the stereoselectivity of free radical reactions can also be directed. Examples involving five- and six-membered cyclic radicals will be used to show how steric and stereoelectronic effects influence the diastereoselectivity of reactions of cyclic radicals with olefins. The temperature, the solvent, and the nature of the radical scavenger used also play a role, so that, if the correct reaction conditions are used, the stereoselectivity of reactions for cyclic reactants can be very high. Lower stereoselectivities are often observed for reactions between acyclic radicals and acyclic alkenes. However, preliminary experiments have indicated that under certain conditions such systems can also react in a stereoselective manner.
    Zusätzliches Material: 9 Tab.
    Materialart: Digitale Medien
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  • 6
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 27 (1988), S. 679-682 
    ISSN: 0570-0833
    Schlagwort(e): Reduction ; Hydrogenation ; Hydrocarbons ; Carbon ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: For the synthesis of organic compounds, reduction is an indispensible reaction type which is also widely used on an industrial scale. In industrial processes hydrogen is usually used as reducing agent, since strong reducing agents like alkali metals and hydrides can only be used to a limited extent for safety and economic reasons. Very economical reducing agents that are convenient to handle and have high potential application are hydrocarbons in presence of carbon. Hydrocarbon/carbon systems can be readily used instead of molecular hydrogen and expensive metal catalysts for the hydrogenation of compounds containing, for example, CC-, CO-, or NO-double bonds. Furthermore, these systems can be used for carrying out reductions which hitherto required strong reducing agents such as zinc, tin, alkali metals and hydrides. Especially suitable as economic sources of hydrogen are refinery products such as vacuum gas oil, fuel oil S or vacuum residue oil. Hydrocarbons are dehydrogenated to unsaturated systems and finally to carbon.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 27 (1988), S. 797-827 
    ISSN: 0570-0833
    Schlagwort(e): Cyclobutanes ; Cyclobutenes ; Synthetic methods ; Natural products ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The chemical reactivity of cyclobutanones and cyclobutenones is considerably different from that of cyclic ketones with larger rings; this is due to their ring strain of ca. 25 kcal/mol. Detailed knowledge regarding the influence of this ring strain on regio-, chemo- and stereoselective transformations of four-membered ring ketones is of particular importance. While several reactions, such as the Baeyer-Villiger reaction, the Beckmann and Favorskii rearrangements and cine-substitution often proceed in a manner specific to four-membered rings, other reactions such as the facile ring-opening by nucleophiles, the rearrangement to tropolones, the thermal [2+2]-cycloreversion, the isomerization to vinylketenes and the photochemical formation of oxacarbenes are rather specific to cyclobutanones and cyclobutenones. The remarkable selectivity and the excellent yields of such transformations, which are favored or caused by ring strain as the inherent driving force, offer the synthetic chemist fascinating possibilities for the development of new strategies for the synthesis of natural products and biologically active compounds.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 27 (1988), S. 1113-1126 
    ISSN: 0570-0833
    Schlagwort(e): Indoles ; Synthetic methods ; Transition metals ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The use of transition-metal complexes as reagents for the synthesis of complex organic compounds has been under development for at least several decades, and many extraordinary organic transformations of profound potential have been realized. However, adoption of this chemistry by the practicing synthetic organic chemist has been inordinately slow, and only now are transition-metal reagents beginning to achieve their rightful place in the arsenal of organic synthesis. Several factors contributed to the initial reluctance of synthetic organic chemists to use organometallic reagents. Lacking education and experience in the ways of elements having d electrons, synthetic chemists viewed organometallic processes as something mysterious and unpredictable, and not to be discussed in polite society. Organometallic chemists did not help matters by advertising their latest advances as useful synthetic methodology, but restricting their studies to very simple organic systems lacking any serious functionality (e.g., the “methyl, ethyl, butyl, futile” syndrome). Happily, things have changed. Organometallic chemists have turned their attention to more complex systems, and more recently trained organic chemists have benefited from exposure to the application of transition metals. This combination has set the stage for major advances in the use of transition metals in the synthesis of complex organic compounds. This review deals with one aspect of this area, the use of transition metals in the synthesis of indoles.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 27 (1988), S. 226-246 
    ISSN: 0570-0833
    Schlagwort(e): Zeolites ; Catalysis ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Zeolites have proved to be valuable technical catalysts in petrochemistry and in oil processing. The characteristic properties of zeolites, such as acidity, shape-selectivity and thermal stability also enable them to be used for highly selective synthesis in the fields of chemical intermediates and fine chemicals. This interesting area of application has grown continuously in recent years. The present article summarizes the various standard types of reaction involved in organic syntheses which can be catalyzed by zeolites; these include, inter alia, electrophilic and nucleophilic substitution reactions, isomerization of double bonds and carbon skeletons, as well as addition, elimination and hydrogenation reactions.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 10
    ISSN: 0570-0833
    Schlagwort(e): Ketenimines ; Carbene ligands ; Isocyanides ; Carbocycles ; Heterocycles ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Ketenimine complexes are readily available in great variety by reaction of isocyanides with carbene complexes. They have proven to be useful building blocks in new synthetic approaches to carbocyclic and N-heterocyclic four-, five-, and six-membered rings. The reactions involve new metal-induced bond formation patterns of the ketenimine ligands, which can be influenced across a wide range by varying the following five parameters: the metal, the ligands, and the three substituents on the N=C=C unit.
    Zusätzliches Material: 8 Tab.
    Materialart: Digitale Medien
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  • 11
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 27 (1988), S. 1484-1508 
    ISSN: 0570-0833
    Schlagwort(e): Phosphaalkynes ; Synthetic methods ; Phosphorus-carbon compounds ; Multiple bonds ; Heterocycles ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Organophosphorus compounds have been applied in two ways in chemical synthesis. They can either be used as a reagent in a step of the synthesis (for example, in the Wittig reaction) or they can be incorporated directly into the target molecule. This second application, in particular, has expanded greatly in the last few years with the preparation of low-coordination phosphorus compounds. These include the phosphaalkynes, which are of great interest to organic and inorganic chemists. Phosphaalkynes have been employed in the synthesis of heterocyclic compounds, phosphaarenes and their valence isomers, and polycyclic compounds. Further applications have been the use of phosphaalkynes as new ligand systems in complex chemistry and their cyclooligomerization with organometallic reagents. While the chemical properties of phosphaalkynes have little in common with those of nitriles, they are in many ways very similar to those of the isoelectronic acetylenes.
    Zusätzliches Material: 4 Tab.
    Materialart: Digitale Medien
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  • 12
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 27 (1988), S. 622-642 
    ISSN: 0570-0833
    Schlagwort(e): Synthetic methods ; Enzyme catalysis ; Fermentation ; Biotechnology ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: In recent years, the most significant development in the field of synthetic organic chemistry has been the application of biological systems to chemical reactions. Reactions catalyzed by enzymes and enzyme systems display far greater specificities than more conventional organic reactions. Biological and/or enzymatic syntheses and transformations, that is, “microbial transformations,” have great potential. Some of these reactions have already been shown to have useful applications in the fields of synthetic organic chemistry and biotechnology. This article reviews the current status of the rapidly developing field of microbial transformation, the methodology, available technological procedures, and fields of application being described especially in relation to conventional organic synthesis methods.
    Zusätzliches Material: 16 Ill.
    Materialart: Digitale Medien
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  • 13
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 26 (1987), S. 15-23 
    ISSN: 0570-0833
    Schlagwort(e): Monosaccharides ; Synthetic methods ; Carbohydrates ; Heptoses ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The evolution of a strategy to synthesize the title compounds is described. Three principal developments allowed realization of this goal: (1) the attainment of high margins of diastereofacial selectivity and regioselectivity in the construction of pyranoid systems via the Lewis acid-catalyzed cyclocondensation reaction of activated dienes and aldehydes; (2) the exploitation of stereoselective reactions for functionalization of the pyranoid matrix; and (3) the discovery of stereoselective reactions for extending the chiral biases of pyranoid systems to newly emerging stereogenic centers on side chains. The coordination of these components in the synthesis of target systems of high biological interest is described.
    Zusätzliches Material: 18 Ill.
    Materialart: Digitale Medien
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  • 14
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 26 (1987), S. 190-203 
    ISSN: 0570-0833
    Schlagwort(e): Homogeneous hydrogenation ; Hydrogenation ; Synthetic methods ; Catalysis ; Stereoselectivity ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Stereochemical control is a major concern in the application of homogeneous catalysis to organic chemistry. In this context, the directed hydrogenation of olefins employing cationic rhodium or iridium catalysts has considerable potential, for very high selectivity can be attained under mild reaction conditions. The only requirement is a polar functional group in proximity to the double-bond which remains bound to the metal during the catalytic cycle and thereby controls the Stereochemical course of hydrogen delivery through the constraints of chelation. The substituent is most frequently a hydroxy group OH but can also be an ester, amide or carbamate group; other groups remain to be scrutinized. In cyclic compounds, directed hydrogenation can lead to face-selectivity, and the polar substituent may be in the β-, γ-, or δ-position to the double-bond. Acyclic stereoselection ensues with β- or γ-substituents in appropriate compounds, and the configuration of reduced product is predictable on the basis of simple rules. The application of optically active rhodium complexes leads to useful kinetic resolution procedures.
    Zusätzliches Material: 12 Ill.
    Materialart: Digitale Medien
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  • 15
    ISSN: 0570-0833
    Schlagwort(e): Glycopeptides ; Molecular recognition ; Molecular recognition ; Synthetic methods ; Carbohydrates ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Glycopeptides are partial structures of the connecting regions of glycoproteins and, like these, always contain glycosidic bonds between the carbohydrate and peptide parts. Glycoproteins are not only widely distributed but are also decisive factors in post-translational biological selectivity, especially in biological recognition. Targeted syntheses of glycopeptides require stereoselective formation of the glycosidic bonds between the carbohydrate and the peptide parts and protective group methods that enable selective deblocking of only one functional group in these polyfunctional molecules. These heavy demands have been met by the well-established use of benzylic protective groups, which can be removed by hydrogenolysis, combined with the use of base-labile 2-phosphonioethoxycarbonyl (Peoc) or 9-fluorenylmethoxycarbonyl (Fmoc) protective groups or of bromoethyl esters, which can be removed under neutral conditions. The acidolysis of tert-butyloxycarbonyl (Boc) groups and of tert-butyl esters has also been successfully used, although, under acidic conditions, anomerization or rupture of the glycosidic bonds may occur, especially when nucleophiles are present. The stable, two-stage 2-(pyridyl)ethoxycarbonyl (Pyoc) protective groups allow a more reliable synthesis of complex glycopeptides since they can be removed, after modifications, under mild conditions. Particularly suitable for the synthesis of sensitive glycopeptides are the stable allyl protective groups. They can be removed from the complex glycopeptides in a highly selective and effective manner by means of noble-metal catalysts under practically neutral conditions. These methods have been employed to synthesize glycopeptides corresponding to partial structures of interesting glycoproteins. Deprotected glyopeptides representing tumor-associated antigen structures can be coupled to bovine serum albumin, which serves as a biological carrier molecule, without the necessity of using an artificial coupling component (spacer).
    Materialart: Digitale Medien
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  • 16
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 26 (1987), S. 24-37 
    ISSN: 0570-0833
    Schlagwort(e): Stereoselective aldol reactions ; Aldol reaction ; Chiral enolates ; Enolates ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The aldol reaction is among the most important methods of forming carbon-carbon bonds. The addition of an enolate to an aldehyde leads to the formation of at least one chiral center. In the case of α-substituted enolates it has to a large extent been possible to control the product stereochemistry, while the aldol reaction of α-unsubstituted chiral enolates was for many years a “problem child” for synthetic chemists because of its insufficient stereoselectivity. Progress in this area has only been made in the last few years using either new chiral auxiliaries or alternatives to the aldol reaction.
    Materialart: Digitale Medien
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  • 17
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 26 (1987), S. 204-217 
    ISSN: 0570-0833
    Schlagwort(e): Synthetic methods ; Reduction ; Carbanions ; Cycloannelation ; Cycloalkenes ; Polycycles ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The successive reduction of fully conjugated cyclic hydrocarbons leads to singly and multiply charged ions with unusual bonding. The charge distribution in these ions can be determined spectroscopically, and the information so obtained is then used in kinetically controlled trapping reactions for the regioselective introduction of electrophilic groups. When non-benzenoid substrates are used, syntheses become possible which can either not be carried out or can only be carried out with great difficulty in other ways. Examples of new preparative applications are cycloannelation and bridging reactions as well as polymerization reactions. The ion pair structure of the intermediate and the type of electrophile used are of paramount importance in controlling the mechanism of these reductive transformations.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 18
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 26 (1987), S. 489-503 
    ISSN: 0570-0833
    Schlagwort(e): Natural products ; Synthetic methods ; Polyketides ; Stereoselectivity ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Sequences of directly adjacent stereogenic centers were first discovered for the monosaccharides, which therefore constituted the first focus of interest in Stereoselective synthesis. The structures of many polyketide-derived natural products that have been elucidated in recent years often exhibit longer sequences of stereogenic centers in which hydroxy-substituted secondary carbon atoms alternate with tertiary carbon atoms. This finding inspired the development of methods allowing the specific construction of first two and then - more importantly-three neighboring stereogenic centers. The diverse methodologies that have thereby emerged reveal common principles and stress the variety of approaches possible in stereoselective synthesis.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
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  • 19
    ISSN: 0570-0833
    Schlagwort(e): Glycosides ; Oligosaccharides ; Koenigs-Knorr method ; Synthetic methods ; Carbohydrates ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Glycoproteins, glycolipids, and glycophospholipids (glycoconjugates) are components of membranes. The oligosaccharide residue is responsible for intercellular recognition and interaction; it acts as a receptor for proteins, hormones, and viruses and governs immune reactions. These significant activities have stimulated interest in oligosaccharides and glycoconjugates. With their help it should be possible to clarify the molecular basis of these phenomena and to derive new principles of physiological activity. Major advances in the synthesis of oligosaccharides have been made by the use of the Koenigs-Knorr method, in which glycosyl halides in the presence of heavy-metal salts are employed to transfer the glycosyl group to nucleophiles. The disadvantages of this procedure have led to an intensive search for new methods. Such methods will be discussed in this article. Emphasis is placed on glycoside and saccharide formation by 1-O-alkylation, on the trichloroacetimidate method, and on activation through the formation of glycosylsulfonium salts and glycosyl fluorides.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 20
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 25 (1986), S. 414-430 
    ISSN: 0570-0833
    Schlagwort(e): Gas-phase flow thermolysis ; Thermolysis ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The preference for carrying out synthetic organic reactions at the lowest possible temperature is due to the expectation that the selectivity often increases with decreasing temperature, as is confirmed by many examples and also theoretically justified. Selectivity, however, is not the only problem at high temperatures; further factors include the frequently limited thermal stability of the functional groups and structural elements not directly involved in the transformation. In spite of these limitations, the advantages of high temperatures and the greatly improved knowledge of the mechanisms of dynamic gas-phase processes accumulated in recent years can be exploited in directed organic synthesis. In this review the synthetic potential of gas-phase flow thermolysis will be described from the viewpoint of the synthetic chemist with the aid of typical examples of application.
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  • 21
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 25 (1986), S. 508-524 
    ISSN: 0570-0833
    Schlagwort(e): Cross-coupling ; Organotin compounds ; Electrophilicity ; Palladium ; Catalysis ; C-C coupling ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The cross-coupling of organotin reagents with a variety of organic electrophiles, catalyzed by palladium, provides a novel method for generating a carbon-carbon bond. Because this mild, versatile reaction is tolerant of a wide variety of functional groups on either coupling partner, is stereospecific and regioselective, and gives high yields of product, it is ideal for use in the synthesis of elaborate organic molecules. When the coupling reaction is carried out in the presence of carbon monoxide, instead of a direct coupling, carbon monoxide insertion takes place, stitching the two coupling partners together and generating a ketone.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 22
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 25 (1986), S. 960-970 
    ISSN: 0570-0833
    Schlagwort(e): Phase-transfer catalysis ; Catalysis ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The development of Phase Transfer Catalysis (PTC) represents a major step forward in the employment of many organic reactions and renders them very convenient and useful processes. These reactions involve the application of nucleophiles in general, anions and bases in particular, in reactions carried out in a water-organic solvent system. They can be performed both in the laboratory and on an industrial scale. The ease of application of PTC processes is the main reason for their increasing utilization in industry. An outstanding achievement of this technique is the employment of aqueous bases in reactions which traditionally would otherwise require a strong base in a nonaqueous medium. The classical procedures that require severe anhydrous conditions, expensive solvents and dangerous bases such as metal hydrides and organometallic reagents are now replaced by aqueous solutions of, e.g., sodium or potassium hydroxides (PTC/OH processes). In contrast to the extensive synthetic applications of PTC/OH systems, the detailed mechanisms of these processes have been the subject of a great deal of controversy and various mechanisms have been suggested. However, it would seem that our knowledge concerning the mechanistic aspects of such reactions has now reached the stage where it can be used to advantage in synthesis planning. A better understanding of the various factors which influence the reaction would undoubtedly help to optimize PTC/OH processes such as to enable higher yields in shorter reaction times at lower temperatures. The importance of, inter alia, the catalyst will be pointed out and it is highly recommended that such catalysts be always available in the laboratory, for the range of organic reactions that they can efficiently, conveniently and safely catalyze is vast indeed.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 23
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 25 (1986), S. 1-20 
    ISSN: 0570-0833
    Schlagwort(e): Cycloaddition ; Trimethylenemethane ; Synthetic methods ; Cyclopentanes ; Heterocycles ; Natural products ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The power of cycloadditions for ring formation derives from the potential for chemo-, regio-, diastereo-, and enantioselectivity. Trimethylenemethane (TMM) and its equivalents offer the possibility of extending such benefits to the synthesis of five-membered rings. Three types of conjunctive reagents appear to be promising candidates: (1) selected 4-alky-lidene-4,5-dihydro-3H-pyrazoles, (2) 2-[(trimethylsilyl)methyl]allyl esters and halides, and (3) alkylidenecyclopropanes. Thermal reactions, especially intramolecular ones, effect the cycloaddition of the pyrazoles to olefins-especially electron-poor olefins. The latter two precursors require a catalyst, notably a palladium complex, to unlock the synthetic potential. With the 2-[(trimethylsilyl)methyl]allyl esters, a general chemo-, regio-, and diastereoselective cycloaddition with typical Diels-Alder dienophiles forms methylenecyclopentanes in both inter- and intramolecular fashion. A tin analogue allows extension of this cycloaddition to aldehydes, and, in a related sequence, to ketones and imines to form 3-methylenete-trahydrofurans and 3-methylenepyrrolidines with excellent diastereoselectivity. The 2-[(tri-methylsilyl)methyl]allyl esters also serve to effect net methylenecyclopentane annulation to cyclic enols. Such adducts can further undergo three-carbon intercalation or combined ring contraction-spiroannulation simply by the use of either a nucleophilic or electrophilic trigger. Alkylidenecyclopropanes undergo cycloadditions to both electron-rich and electron-poor olefins when stimulated by metal catalysts, especially palladium. A complementary regiochemistry to the approach based upon silicon conjunctive reagents is observed. The availability of these cycloadditions provides new strategies for the synthesis of natural products.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
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  • 24
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 25 (1986), S. 683-701 
    ISSN: 0570-0833
    Schlagwort(e): Electroorganic synthesis ; Electrochemistry ; Synthetic methods ; Redox chemistry ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The electrochemical formation and regeneration of redox agents for organic syntheses (indirect electrolysis) widens the potential of electrochemistry, as higher or totally different selectivities can often be obtained while at the same time the energy input can be lowered significantly. Higher current densities can also be obtained by preventing otherwise often encountered electrode inhibition. New types of redox catalysts can be formed in-situ and can be regenerated after reaction with the substrates. This principle is of increasing importance also for the application of already known redox agents with regard to environmental protection, since large amounts of a product can be generated in a closed circuit using only relatively small amounts of the redox reagent. Consequently the operation of such a process can be greatly simplified, and the release of ecologically objectionable spent reagents into the environment can be prevented. The broad spectrum of redox catalysts currently in use includes, inter alia, metal salts in very low or high oxidation states, halogens in various oxidation states, and, in particular, a wide variety of transition-metal complexes. A great deal of progress has recently been made in the application of organic electron transfer agents, since compounds have been found that are sufficiently stable in both the reduced as well as the oxidized state.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 25
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 25 (1986), S. 790-807 
    ISSN: 0570-0833
    Schlagwort(e): Anthracyclinones ; Synthetic methods ; Antibiotics ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The remarkable antitumor properties of anthracycline antibiotics have motivated synthetic chemists, and a large number of groups have been active recently in this field. Initially, there was very little hope for this class of substances due to their extreme toxicity. However, the dividing line between toxicity and desired pharmacological effect has broadened to such an extent, partly through microbiological methods (new strains, mutants) and partly through semisynthetic modifications, that today anthracyclines take number one place (over 20% of the market) in the chemotherapy of (human) cancer. The demands made on modern cytostatica are extremely high, as may be seen from the fact that of the more than 600000 drugs tested in animals, only about 40 are in clinical use. In the meantime, some anthracyclines obtained by total synthesis are also in clinical testing. In this review it will hopefully be demonstrated that all those concerned in the chemotherapeutic use of these substances have also contributed to the general progress made in the solution of regio- and stereo-chemical problems of linearly annelated ring systems.
    Materialart: Digitale Medien
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  • 26
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 25 (1986), S. 947-959 
    ISSN: 0570-0833
    Schlagwort(e): Lewis acids ; Synthetic methods ; Selectivity ; Organocopper compounds ; Addition ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Organometallic compounds with pronounced nucleophilicity such as organocopper and organolithium compounds, and powerful electrophiles, such as BF3 and AlCl3, are generally thought to be incompatible under normal, homogeneous reaction conditions. As a matter of course, it is anticipated that the two species cannot coexist and undergo transmetalation reactions. To our surprise, however, RCu and BF3 are compatible at low temperature. RCu·BF3 and related organocopper-Lewis acid reagents exhibit new and unique reactivities and selectivities: in conjugate additions, e.g., not only activation but also high regio-, stereo-, and chemo-selectivity as well as very high asymmetric induction is observed; allylic derivatives are alkylated regioselectively, and reaction towards carbonyl groups, imines, epoxides, aziridines, ethers, acetals, orthoformates, and pyridinium salts is in each case found to be selective. RLi·BF3 and related organolithium-Lewis acid reagents also exhibit noteworthy selectivities and reactivities. These complex reagents are utilized in the key steps of the total synthesis of many important natural products, such as certain terpenes, steroids, and alkaloids.
    Zusätzliches Material: 5 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 27
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 24 (1985), S. 539-553 
    ISSN: 0570-0833
    Schlagwort(e): Chirality ; Reduction ; Synthetic methods ; Enzymes ; Biotechnology ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: It has been known for many decades that chiral compounds can be obtained by stereospecific biocatalytic reduction. Further significant methodological developments in this field have, however, only been made during the past ten years; they include the application of previously unused microorganisms and electron donors, the discovery of additional substrates for the known reductases, the development of methods for regenerating reduced pyridine nucleotides, and the discovery of new reductases which were sought for specific preparative purposes. Many chiral compounds can now be synthesized by microbial hydrogenation using H2 and hydrogenase-containing microorganisms as well as by electromicrobial or electroenzymatic reduction. In the two latter methods, anaerobic or aerobic organisms are supplied with electrons from electrochemically reduced, artificial mediators, e.g., methyl viologen. Reductases that do not require pyridine nucleotides and can accept electrons directly from reduced viologens are especially useful. Two examples of this type of enzyme are described which are of preparative interest. Many cells contain methyl viologen-dependent NAD(P) reductases, a large number of which have still not been characterized. A productivity number is proposed which allows different methods of bioconversion with microorganisms to be compared. The productivity numbers of compounds synthesized by the methods described in this review are often 10- to 100-fold higher than those of substances obtained by conventional techniques.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 28
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 24 (1985), S. 553-565 
    ISSN: 0570-0833
    Schlagwort(e): Free radicals ; Organomercury compounds ; Synthetic methods ; Organotin compounds ; C-C coupling ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: C—C bond formation is one of the most important synthetic steps in the construction of organic molecules. In the last few years it has been increasingly achieved by radical addition to alkenes. In such reactions the adduct radicals have to be trapped by an donor subsequent to the C—C bond formation in order to prevent polymerization. This task can be accomplished with organotin and organomercury hydrides, the use of which has led to new synthetic methods. The occurrence of radical chain reactions in which reactions take place between radicals and nonradicals is decisive for the success of the synthesis. In these cases small amounts of radical initiators suffice and numerous functional groups may be used in the C—C bond-forming reactions. The yields and selectivities of these radical reactions are often very high.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 29
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 24 (1985), S. 617-638 
    ISSN: 0570-0833
    Schlagwort(e): Enzyme catalysis ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Enzymes have great potential as catalysts for use in synthetic organic chemistry. Applications of enzymes in synthesis have so far been limited to a relatively small number of largescale hydrolytic processes used in industry, and to a large number of small-scale syntheses of materials used in analytical procedures and in research. Changes in the technology for production of enzymes (in part attributable to improved methods from classical microbiology, and in part to the promise of genetic engineering) and for their stabilization and manipulation now make these catalysts practical for wider use in large-scale synthetic organic chemistry. This paper reviews the status of the rapidly developing field of enzyme-catalyzed organic synthesis, and outlines both present opportunities and probable future developments in this field.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 30
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 24 (1985), S. 668-682 
    ISSN: 0570-0833
    Schlagwort(e): Organoaluminum compounds ; Synthetic methods ; Selectivity ; Beckmann rearrangement ; Rearrangement ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: In addition to their high oxyphilicity, organoaluminum compounds are endowed with ambiphilic character. These properties can be successfully utilized in developing new synthetic reactions with unique selectivities. Especially noteworthy are the organoaluminum-promoted Beckmann rearrangement of oxime sulfonates, new syntheses of polyamino macrocycles via reductive cleavage of aminals and amidines by diisobutylaluminum hydride, the diastereoselective cleavage of chiral acetals by organoaluminum compounds leading to optically active secondary alcohols, allylic alcohols, and β-substituted carbonyl compounds, and biomimetic terpene syntheses. These and other examples, which illustrate the characteristics of organoaluminum chemistry, are used to demonstrate the distinct advantages of organoaluminum reagents in selective organic synthesis.
    Zusätzliches Material: 11 Tab.
    Materialart: Digitale Medien
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  • 31
    ISSN: 0570-0833
    Schlagwort(e): Quinones ; Quinones ; Michael addition ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: If catechol or other hydroquinones are dehydrogenated in the presence of a nucleophilic reagent, the latter reacts, usually by Michael addition, with the quinone formed in situ. The wide range of possible variations offered by this synthetic method is comprehensively described in the present paper. procedures are given for carrying out typical reactions.
    Materialart: Digitale Medien
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  • 32
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 3 (1964), S. 250-260 
    ISSN: 0570-0833
    Schlagwort(e): Unsaturated fatty acids ; Fatty acids ; Carbonyl olefination ; Synthetic methods ; Wittig reactions ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: It is shown that carbonyl olefination, i.e. the reaction of carbonyl compounds with alkylidene phosphoranes, can be sterically controlled. In some cases cis-olefins can be obtained by proper choice of the reaction conditions; trans-olefins are formed only in the presence of suitable structural factors. These cis-and trans-olefination reactions have opened new, stereo-specific routes to unsaturated and polyunsaturated fatty acids with differing positions and sequences of cis- and trans-double bonds and to ω-hydroxy and branched chain fatty acids.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
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  • 33
    ISSN: 0570-0833
    Schlagwort(e): Cyclization ; Dialdehydes ; Nitromethane ; Carbohydrates ; Polyalcohols ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Condensation of nitromethane with suitable diadehydes in alkaline medium provides a general method of cyclization, in which the methyl group of the nitromethane is incorporated into the ring. This method leads to 5-, 6-, and 7-membered rings and is equally applicable to aliphatic, aromatic, and sugar dialdehydes. For example, glyoxal is converted into 1,4-dideoxy-1,4-dinitro-neo-inositol, and glutaraldehyde into trans-2-nitrocyclohexane-1,3-diol, while the corresponding cyclization of xylo-trihydroxyglutaraldehyde leads to deoxy-nitroinositols having the scyllo, myo-1, and muco-3 configurations.-In the case of aromatic dialdehydes, the cyclization is accompanied by elimination of water. Thus, phthalaldehyde, naphthalene-2,3-dicarboxaldehyde, and homophthalaldehyde yield, respectively, 2-nitroindenol, 2-nitrobenzindenol, and 2-nitronaphthalene. -Application of the method to sugar dialdehydes (aldehydic diglycol derivatives of monosaccharides formed by periodate oxidation) constitutes an excellent synthesis of 3-amino sugars, since 3-deoxy-3-nitropyranoses are formed smoothly on cyclization, and the corresponding 3-amino derivatives are obtained by hydrogenation. Thus, the reaction sequence: periodate oxidation → cyclization with nitromethane → hydrogenation, leads in the case of α-and β-D-pentosides to 3-amino-3-deoxy-D-and-L-pentosides, respectively, with ribo, xylo, and arabino configurations. α-D-hexosides give derivatives with gluco, manno, and galacto configurations. 3-Amino-3,6-dideoxyglucosides of the D-and L-series are obtained from 6-deoxy-D-or-L-hexosides, respectively, and 3-aminohexosans with gulo, ido, and altro configurations are obtained from 1,6-anhydro sugars. Cyclization of the dialdehydes obtained from sedoheptulose and methyl 4,6-O-ethylidene-α-D-glucoside by periodate oxidation, leads to 3-nitro and, after hydrogenation, to 3-amino derivatives of 3-deoxyheptopyranoses.
    Materialart: Digitale Medien
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  • 34
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 2 (1963), S. 24-29 
    ISSN: 0570-0833
    Schlagwort(e): 3-Aminoquinazol-4-one ; 3-Aminobenzotriazin-4-one ; Quinazolones ; Benzotriazinones ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Among the derivatives of 3-aminoquinazol-4-one and 3-aminobenzotriazin-4-one are compounds with narcotic, sedative, analgetic, and muscle-relaxant properties. Of special interest are compounds with one or several urethane groups and those substituted in the 3-position by a morpholine moiety.
    Zusätzliches Material: 4 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 35
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 2 (1963), S. 225-238 
    ISSN: 0570-0833
    Schlagwort(e): Pyridinium salts ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: This review discusses syntheses leading to a new type of N-vinylpyridinium salts, to novel anionocyanines, to aminophenazines and alloxazines, as well as to (aza-) dehydroquinolizinium, acridizinium, and morphanthridizinium salts. In addition, Mannich reactions and aminoalkylations at active methylene groups of cycloimmonium salts, and their reactions with amines are treated. The possibilities offered by the “Ortoleva-King” reaction are demonstrated using numerous examples, such as a new route leading to the yohimbine skeleton.
    Materialart: Digitale Medien
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  • 36
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 2 (1963), S. 309-323 
    ISSN: 0570-0833
    Schlagwort(e): s-Triazines ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The preparation and properties of s-triazine are discussed. Nucleophilic reagents (even water) readily attack s-triazine. Thus, open-chain and heterocyclic compounds, e.g. formamidines, aminomethylene compounds, and triazole, pyridine, and pyrimidine deravatives are accessible from s-triazine. With amidines and imido ethers substituted triazines are obtained (by trans-triazination).The latter are formed via open-chain intermediates.
    Zusätzliches Material: 11 Tab.
    Materialart: Digitale Medien
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  • 37
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 2 (1963), S. 380-393 
    ISSN: 0570-0833
    Schlagwort(e): Pyridinium salts ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Cleavage of N-phenylpyridinium or N-vinylpyridinium salts with secondary aliphatic amines leads to aromatic amino compounds or enamines which are often unobtainable by other routes. The other fragment, glutacondialdehyde or its monoanil, gives azulenes, as shown by Ziegler and Hafner, as well as König; these compounds can also be prepared from alkylpyridinium salts with cyclopentadienylsodium (Hafner). Syntheses of labile aldehydes which are otherwise difficult to obtain and of α-ketocarboxylic acids, starting from pyridinium salts and proceeding via nitrones or α-cyanoanils, are illustrated by many new examples. Benzimidazoles, benzothiazoles, and amidines are accessible from pyridinium salts via nitrones or α-cyanoanils; cyanoanils can be transformed into quinoxalines (including xanthopterine), perimidines, etc. Furthermore, nitrosonaphthols and nitrosonaphthylamines react with pyridinium salts containing an active methylene group on the nitrogen, leading to new ring systems. Further synthetic possibilities arise from nucleophilic displacements of the pyridine in pyridinium salts by SN 2 reactions. Combination of the route via nitrones with the methods of Arndt-Eistert, Ortoleva-King, or with chloromethylation constitutes a significant enlargement of its range of application. The formation of α-cyanoanils from diazoketones permits synthesis of α-keto-β-amino acids from α-amino acids, or of phenylglyoxylic acids from benzoic acids by chain extension.
    Materialart: Digitale Medien
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  • 38
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 1 (1962), S. 8-21 
    ISSN: 0570-0833
    Schlagwort(e): Addition ; Immonium ions ; Isocyanides ; Amino acids ; Synthetic methods ; Alkylidene ammonium ions ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The α-addition of immonium ions and anions (OH-, SeH-, S2O3 2-, N3- NCO- NCS-, R—CO2 -, RO—CO2-) to isonitriles, accompanied by secondary reactions provides a means for the one-stage synthesis of organic nitrogen compounds starting with two to five different components. Thus, by the condensations of amines (ammonia, primary, and secondary aliphatic and aromatic amines, hydrazines) and aldehydes or ketones with isonitriles and acids, a number of α-aminocarboxylic acid amides, thioamides, selenoamides, 1,5-disubstituted retrazoles, hydantoin imides, thiohydantoin imides, α-acylamino carboxylic acid amides, oligopeptide derivatives, β-lactams, derivatives of penicillanic acid, urethanes, diacylimides, and various hydrazine derivatives, can be prepared. The reactions are easily carried out and take place under mild conditions. Yields of more than 90% are frequently encountered.
    Zusätzliches Material: 4 Tab.
    Materialart: Digitale Medien
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  • 39
    ISSN: 0570-0833
    Schlagwort(e): Amides ; Azolides ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 40
    ISSN: 0570-0833
    Schlagwort(e): Michael addition ; Pyridinium salts ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: By Michael addition of the active methylene groups in pyridinium salts onto suitable acceptor compounds, α-pyridones, substituted pyridines, particularly pyridinecarboxylic acids and pyridylpyridines, including the minor alkaloid of tobacco nicotelline and annelized pyridines, can be prepared by a simple procedure and generally in good yields. From the Michael adducts, polycyclic aromatic hydrocarbons, e.g. substituted fluoranthenes and “bisfluoranthenes” can be prepared; internal Michael addition leads to pyrrolinopyrdinium salts. For example, Michael addition of pyridinium salts onto quinones gives phenacyl substituted quinones, from which benzofurans and cinnolines can be readily obtained.
    Materialart: Digitale Medien
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