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  • 1975-1979  (30)
  • 1960-1964  (10)
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  • 1910-1914
  • Synthetic methods
  • 1
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 18 (1979), S. 707-721 
    ISSN: 0570-0833
    Schlagwort(e): Onium compounds ; Aza-arenes ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Effective syntheses employing 2-halogenated pyridinium, benzoxazolium, benzothiazolium, and pyridinium salts have been accomplished in the absence of strong acids and bases. Activation of carboxylic acids or alcohols with these onium salts leads to 2-acyloxy and 2-alkoxy intermediates which can be transformed into esters, amides, thiol esters, (macrocyclic) lactones, acid fluorides, olefins, allenes, carbodiimides isocyanates, isothiocyanates, nitriles, and isocyanates. The possibility of performing stereospecific syntheses (involving configurational inversion) with onium salts deserves attention.
    Zusätzliches Material: 20 Tab.
    Materialart: Digitale Medien
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  • 2
    ISSN: 0570-0833
    Schlagwort(e): Donor-acceptor systems ; Substituent effects ; Free radicals ; Radicophiles ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The 100 yers old Wurster's salts have long been recognized as compounds with redical cations. Their unusual stabilization derives partly form capto-dative (cd) substitution. This principle is now discussed as one factor of radical stabilization and it is applied to simple methine derivatives. cd-Substitution has synthetically useful applications: cd-substituents on a carbon atom allow its selective dehydrodimerization. Olefines with geminal and thus cross-conjugated cd-substituents are “radicophilic” and permit twofold carbon radical addition. cd-Substituted olefines are useful antioxidants, polymerization inhibitors and are promising agents in the control of biological radical reactions. Generally, many reactions of cd-substituted molecules appear to involve radicals.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 18 (1979), S. 421-429 
    ISSN: 0570-0833
    Schlagwort(e): Triphase catalysis ; Catalysis ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Triphase catalysis (TC) has recently been introduced as a unique form of heterogeneous catalysis in which the catalyst and each of a pair of reactants are located in separate phases. Based on this concept, new synthetic methods have been developed for aqueous phase-organic phase reactions using a solid phase catalyst. Although it is only at an early stage of development, TC shows considerable potential for practical use. Our mechanistic understanding of these highly complex catalytic systems is at present very limited and detailed examination will be required before their relationship to phase-transfer, micellar, and interfacial catalysis becomes clear.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 18 (1979), S. 515-529 
    ISSN: 0570-0833
    Schlagwort(e): Pyrolysis ; Sulfones ; Synthetic methods ; Ring contraction ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Cyclic sulfoness containing structural elements such as aromtic rings, heteroatoms. functional groups, and further SO2-groups as ring members decompose on heating with cleavage of SO2 and formation of a new C—C bond. In the last decade this “sulfone pyrolysis” has been expanded into a generally applicable method even allowing the synthesis of sterically strianed medium-membered and multi-membered cyclic and polycyclic systems containing aromatic ring. By the pyrolysis of sulfones which are only unilateally activated by benzyl moieties, aromatic systms can be bridged by —(CH2)n chains of any desired length. In addition, —(CH2)— chains can be split off together with two SO2 molecules, with recombination of the remaining centers, resulting in ring contraction by four to n atoms. However, sulfone pyrolysis is of importance not only as a ring-contraction method but as a crucial final step in the synthesis of multi-membered hydrocarbon cycles, e.g. of the phane type.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 18 (1979), S. 837-846 
    ISSN: 0570-0833
    Schlagwort(e): C-C coupling ; Synthetic methods ; Catalysis ; Silanes ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The reagent hydrosilane/carbon monoxide opens up new possibilities for organic synthesis. Four cases will be discussed: 1. The reaction of olefins with hydrosilane (trialkylsilane) and carbon monoxide in the presence of Co, Ru, and Rh complexes leads to enol silyl ethers having one more carbon atom that the olefins. 2. Cyclic ethers underto carbonylative ring opening to ω-siloxyaldehydes when reacted with hydrosilane and carbon monoxide in the presence of Co2(CO)8 as catalysts 3. Aldehydes are catalytically converted into the next higher α-siloxyaldehydes or 1,2-bis(siloxy)alkenes depending on the reaction conditions used. 4. The reaction of alkyl acetates proceeds in various ways depending on the nature of the alkyl group; enol silyl ethers or alkenes are optained.-Mechanisms of these Co2(CO)8 catalyzed reactions using hydrosilane and carbon monoxide are discussed in which HCo(CO)n or R3SiCo(CO)nL function as catalytically active agents. With these species there are four types of catalytic cycles.-The synthetic possibilities of these catalytic reactions have still not been fully explored.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
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  • 6
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 18 (1979), S. 900-917 
    ISSN: 0570-0833
    Schlagwort(e): Arylnitrene chemistry ; Synthetic methods ; Nitrenes ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Aryl- and heteroaryl-nitrenes can take part in intra-and intermolecular reactions in both of their possible electronic states (triplet and singlet). In this review we have endeavored to high-light recent synthetic uses of these reactive intermediates as well as draw attention to avenues open to further exploration in this field. Singlet arylnitrenes will interact with suitable ortho-positioned substituents to give a variety of fused azoles, some in excellent yield. In suitable solvents and in presence of amines and alcohols, phenylnitrenes undergo ring expansion to azepines which can also occur in nitrenes of certain fused bicyclic aromatics (naphthalene, quinoline, isoquinoline, benzo[b]thiophene). The latter nitrenes may also give rise to o-diamines which are useful starters for further heterocyclic synthesis. Triplet arylnitrenes (usually regarded as having only a nuisance effect in synthetic work) may also be utilized in practicable heterocyclic syntheses within a suitable molecular framework. Decomposition of aryl azides in a mixture of an organic and polyphosphoric acid leads to fused oxazoles. The mechanism is discussed for all the reactions considered.
    Zusätzliches Material: 8 Tab.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 17 (1978), S. 169-175 
    ISSN: 0570-0833
    Schlagwort(e): Organoaluminum compounds ; Selectivity ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: With the aid of selected examples an overview is given of the development trends in highly discriminative reactions using organoaluminum compounds. (1) Isomerization of substituted oxiranes into allyl alcohols has been effected both stereo- and regioselectively by means of a new organoaluminum reagent, diethylaluminum 2,2,6,6-tetramethylpiperidide (DATMP); this reaction which provides a new route for the regiospecific transformation of allyl alcohols into 1,3-dienes. (2) A novel nonenzymic heterolysis of allylic phosphates of terpenoids has been effected by organoaluminum compounds and has enabled development of a new method for the selective synthesis of cyclic terpenes. (3) The reductive condensation of α-haloketones with carbonyl compounds in the presence of diethylaluminum chloride and zinc affords β-hydroxy-carbonyl derivatives in good yields with exclusion of undesired self-condensations products.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 17 (1978), S. 476-486 
    ISSN: 0570-0833
    Schlagwort(e): Intramolecular reactions ; Ene reaction ; Synthetic methods ; Cyclization ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Thermal cyclizations of appropriate dienes, enynes and related unsaturated systems, some of them carried out on an industrial scale, demonstrate increasingly the preparative power of the intramolecular ene reaction. A variety of substituted, fused and bridged ring systems, including natural products, are thus easily accessible in a regio- and stereo-selective manner. Numerous examples are discussed systematically illustrating the possibilities, limitations, and common features of this cyclization reaction and its reverse ring-opening process.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 17 (1978), S. 487-496 
    ISSN: 0570-0833
    Schlagwort(e): Alumina surfaces ; Synthetic methods ; Surface chemistry ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Recent examples are given to emphasize that alumina can cause many different and often unexpected chemical reactions of adsorbed organic molecules. Recent developments are summarized to publicize that reagent-doped alumina can be used deliberately to achieve some very mild and highly selective organic transformations. The scope and limitations of organic reactions at alumina surfaces are discussed, and the advantages of these heterogeneous reactions over the corresponding homogeneous ones are pointed out. The role of the alumina and future problems are discussed briefly.
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 17 (1978), S. 505-515 
    ISSN: 0570-0833
    Schlagwort(e): Pyridines ; Alkynes ; Nitriles ; Synthetic methods ; Cobalt catalysts ; Catalysis ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Soluble organocobalt catalysts permit selective formation of substituted pyridines under mild conditions in a single step: mono-, di-, and trisubstituted pyridines can be obtained at will in high conversions and high yields from nitriles and alkynes. Polynuclear derivatives such as bipyridines can also be prepared by this method.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 11
    ISSN: 0570-0833
    Schlagwort(e): 4-Dialkylaminopyridines ; Amino pyridines ; Acylation ; Catalysis ; Synthetic methods ; Pyridines ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The synthesis of 4-dialkylaminopyridines can be accomplished in two steps starting from pyridine. Compared to pyridine, these derivatives are approximately 104 times more active when used as acylation catalysts. Dialkylaminopyridines are being used with ever-increasing frequency for acylation reactions which proceed either incompletely or not at all in pyridine. This article reviews the various possible applications of 4-dialkylaminopyridines in terpene, steroid, carbohydrate and nucleoside chemistry as well as in the transformation of amino acids into α-acyl aminoketones and polymerization of isocyanates. In addition, N-substituted 4-dialkylaminopyridinium salts can be used for the transfer of sensitive groups to nucleophiles in aqueous medium. The exceptional catalytic effect of these derivatives, even in non-polar solvents, is due, in part, to the formation of high concentrations of N-acylpyridinium salts which are present in solution as loosely-bound, highly reactive ion pairs.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 12
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 17 (1978), S. 27-37 
    ISSN: 0570-0833
    Schlagwort(e): Organomercury compounds ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Organomercurials have been known since 1850 and many synthetic routes to these compounds presently exist. The ability of these compounds to accommodate a wide variety of functional groups and to tolerate quite diverse reaction conditions makes them attractive as synthetic intermediates. While the solvomercuration-demercuration and divalent carbon transfer reactions remain the most widely used of the organomercurial reactions, a number of new synthetic procedures employing organomercurials have been developed in recent years. Many of these involve transmetallation reactions with palladium salts.
    Materialart: Digitale Medien
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  • 13
    ISSN: 0570-0833
    Schlagwort(e): Oxygenation ; Alkanes ; Synthetic methods ; Superacidic systems ; Catalysis ; Magic acid ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Owing to the ready availability of the starting materials, the functionalization of saturated hydrocarbons for preparing chemical intermediates and products represents an attractive goal. The possibility of converting alkane in a controlled way into alcohols, ketones etc., i.e. to oxyfunctionalize them, is particularly challenging. After a short account of previous methods used for the oxidation of alkanes, particular emphasis will be given to recently developed reactions of alkanes with oxygenating agents in superacidic media.
    Zusätzliches Material: 16 Tab.
    Materialart: Digitale Medien
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  • 14
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 16 (1977), S. 10-23 
    ISSN: 0570-0833
    Schlagwort(e): Cycloaddition ; Synthetic methods ; Intramolecular reactions ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Numerous examples of intramolecular cycloaddition of 1,3-dienes, nitrones, and azomethine imines attest the preparative value of this variant for regioselective and stereoselective synthesis of annelated and bridged ring systems. The common features, differences, and limitations of these types of reaction are systematically reviewed.
    Materialart: Digitale Medien
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  • 15
    ISSN: 0570-0833
    Schlagwort(e): Phosphorus ylides ; Ylides ; Phosphorus ylides ; Synthetic methods ; Phosphorus ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Phosphacumulene ylides and phosphaallene ylides are nucleophilic compounds which can add reactants in a variety of ways. Cycloadditions can occur both at the polar C - P ylide bond and at the C=C double bond.
    Zusätzliches Material: 13 Tab.
    Materialart: Digitale Medien
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  • 16
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 16 (1977), S. 365-373 
    ISSN: 0570-0833
    Schlagwort(e): Flash thermolysis ; Thermolysis ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Flash thermolysis is a special form of gas-phase thermolysis that is particularly suitable for the production and isolation of thermolabile reaction products. The theoretical basis and the instrumental requirements of the method are first given, and the preparative importance of flash thermolysis for the synthesis of thioketenes, allenes, arynes, highly strained ring systems, quinodimethanes, and other reactive compounds is then demonstrated with the aid of examples.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 17
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 16 (1977), S. 339-348 
    ISSN: 0570-0833
    Schlagwort(e): α-Metalated isocyanides ; Isocyanides ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Being both nucleophilic and electrophilic, α-metalated isocyanides can add to polar double bonds, forming heterocycles. They are also synthons for α-metalated primary amines. This article describes recent or improved procedures for their use in organic synthesis: (1) In heterocyclic syntheses to give 2-oxazolines, 2-imidazolines, 2-thiazolines, oxazoles and oligooxazoles, thiazoles, triazoles, imidazolinones, pyrroles, 5,6-dihydro-1,3-oxazines and -thiazines, and (via cycloaddition with nitrones) 2-imidazolidinones. (2) In the field of formylaminomethylenation, for example transformation of estrone methyl ether and a keto sugar into the corresponding α-formylaminoacrylic esters, and the conversion of aldehydes and ketones by 3- and 4-pyridyl-methyl isocyanides into N-(1-pyridyl-1-alkenyl)formamides and their hydrolysis to 3- and 4-acylpyridines. (3) In connection with the use of α-metalated isocyanides as synthons for α-metalated primary amines, the author demonstrates how they may be used for preparation of 1,2- and 1,3-amino alcohols, 1,2-diamines, 2,3-diaminoalkanoic acids and for synthesis of higher amino acids starting from simple amino acids.
    Materialart: Digitale Medien
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  • 18
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 16 (1977), S. 493-505 
    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: Phase-transfer catalysis (PTC) has grown into a versatile preparative method in the last few years. The most notable new developments include the use of crown ethers as phase-transfer catalysts and the introduction of solid-liquid PTC. Some representative examples have been selected from the large number of new PTC reactions and some of them are summarized in tables.
    Zusätzliches Material: 11 Tab.
    Materialart: Digitale Medien
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  • 19
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 16 (1977), S. 817-826 
    ISSN: 0570-0833
    Schlagwort(e): Titanium tetrachloride ; Synthetic methods ; Catalysis ; C-C coupling ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Titanium tetrachloride can accelerate numerous organic reactions. Valuable syntheses of, e.g., allyl sulfides, amides, enamines, and ketones are based upon transformations of functional groups with TiCl4. Particular mention should also be made of carbon-carbon linkage with TiCl4 which permits the synthesis of hydroxy ketones and carbonyl compounds of the Michael adduct type. TiCl4 reduced in situ is suitable for the reduction of chloroarenes or the linkage of two aldehyde molecules to give an alkene.
    Zusätzliches Material: 7 Tab.
    Materialart: Digitale Medien
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  • 20
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 15 (1976), S. 333-340 
    ISSN: 0570-0833
    Schlagwort(e): Hydrozirconation ; Synthetic methods ; Zirconium ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Hydrozirconation has recently been developed as a procedure for functionalizing alkenes, alkynes, and 1,3-dienes via organozirconium(IV) intermediates. These intermediates react with a variety of electrophilic reagents to give organic products in high yield. Mechanisms of reactions involved in these sequences are discussed.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 21
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 15 (1976), S. 639-647 
    ISSN: 0570-0833
    Schlagwort(e): Addition ; Aldehydes ; Synthetic methods ; Esters ; Ketones ; Nitriles ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: In the presence of cyanide ions as catalyst, aromatic and heterocyclic aldehydes can be smoothly added to α,β-unsaturated ketones, esters, and nitriles in aprotic solvents to form γ-diketones, 4-oxo carboxylic esters, and 4-oxo nitriles. Thiazolium salts in the presence of bases are also suitable catalysts; they permit not only addition of aromatic and heterocyclic aldehydes but also the addition of aliphatic aldehydes.
    Zusätzliches Material: 9 Tab.
    Materialart: Digitale Medien
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  • 22
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 15 (1976), S. 1-9 
    ISSN: 0570-0833
    Schlagwort(e): Betaines ; Synthetic methods ; Cycloaddition ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The cycloadditions of 3-hydroxy-1-methylpyridinium betaines with electron-deficient olefins have been extended to a variety of 1-substituents in place of methyl. Application of resonance theory and later of quantum chemical methods led to rationalization of preceding results and prediction of new reactions. Thermal additions of 2π- and 6π-electron addends at the 2,6-positions and of 4π-electron addends at the 2,4-positions are described. The cycloadducts are highly interesting potential synthetic building blocks.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 23
    ISSN: 0570-0833
    Schlagwort(e): Synthetic methods ; Dihydrooxazoles ; Oxazoles ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The oxazoline ring system, first prepared in 1884, has only in the last five years been shown to possess considerable utility in the synthesis of a variety of functionalized organic compounds. By appropriate metalation of the 2-alkyl substituent it is possible to prepare a variety of homologated carboxylic acid derivatives, both chiral and achiral. Various other manipulations of the oxazoline ring lead to aldehydes, ketones, lactones, amino acids, thiiranes, and olefins. Due to the inertness of the oxazoline ring system to various reagents (RMgX, LiAlH4, CrO3, mild acid or alkali) it may be utilized as a protecting group for carboxylic acids during the transformations involving the above reagents. Two major new developments in oxazoline chemistry involve (a) the use of a chiral oxazoline as a reagent for asymmetric synthesis of chiral carboxylic acids, lactones, alcohol, thiiranes, and olefins and (b) a new mode of aromatic substitution in which the aryloxazolines act as nucleophilic or electrophilic reagents. This behavior has led to a variety of polysubstituted benzenes and biphenyls which would be inaccessible by classical routes. A variety of examples illustrating the utility of oxazolines indicated above are presented so that the reader may appreciate the vast potential of this simple ring system in synthesis.
    Zusätzliches Material: 15 Tab.
    Materialart: Digitale Medien
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  • 24
    ISSN: 0570-0833
    Schlagwort(e): Umpolung ; Nitrosamines ; Amines ; Synthetic methods ; Nucleophilic reactions ; Aminoalkylation ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: There are basically two kinds of hetero atoms in organic molecules: one kind confers electrophilic character upon the carbon atom to which it is bound, and the other kind turns it into a nucleophilic site. The development of methods permitting transitions between the two resulting categories of reagents has become an important task of modern organic synthesis. The scope of such umpolung of the reactivity of functional groups is discussed for the case of amines as an example. A method of preparing masked α-secondary amino carbanions consists in nitrosation of the secondary amine, followed by metalation of the resulting nitrosamine α-to the nitrogen, reaction with electrophiles, and subsequent denitrosation. Many examples are given for each of these steps which illustrate the wide scope of the overall synthetic operation (electrophilic substitution at the α-C atom of the secondary amine). Preliminary applications and a method for avoiding the handling of nitrosamines are presented, and the report concludes with a brief account of the significance of nitrosamines in the study of carcinogenesis and mutagenesis.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 25
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 14 (1975), S. 473-485 
    ISSN: 0570-0833
    Schlagwort(e): Ring contraction ; Cyclobutanes ; Cyclopropylmethyl compounds ; Ring expansion ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Cyclobutanes and cyclopropylmethyl compounds vicinally disubstituted in appropriate manner by one electron-donating group and one leaving or electron-receiving group undergo extremely facile ring contractions and expansions respectively. Unlike many rearrangements of small-ring compounds and most rearrangements of larger-ring compounds, these reactions usually give a single product in high yield and thus possess real synthetic interest. The subject matter of this progress report is classified according to the substituents in question since the nature of these groups largely determines the conditions under which rearrangement takes place.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
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  • 26
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 14 (1975), S. 528-538 
    ISSN: 0570-0833
    Schlagwort(e): Bredt rule ; Bridgehead alkenes ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: During the past eight years, bridgehead olefins have attracted rapidly increasing attention. In view of their significance with regard to the stereochemistry of alkenes, the study of certain reaction mechanisms, and the nature of the double bond, detailed research into this structural type appears highly desirable. Bridgehead olefins represent connective linkages between olefins in the ground state and species which can arise in the deactivation of photochemically excited alkenes and cycloalkenes and also contribute to our understanding of the structural conditions prevailing during cis-trans isomerization of alkenes.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 27
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 14 (1975), S. 222-231 
    ISSN: 0570-0833
    Schlagwort(e): Phosphorylcarbenes ; Carbenes ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Phosphorylcarbenes, which have become known only recently during synthetic experiments in the field of phosphoryldiazoalkanes, have twofold preparative value. In the first place, they can be used to introduce phosphoryl groups into organic compounds, as in the phosphoryl-cyclopropanation of alkenes or arenes and in the phosphorylcyclopropenation of alkynes. Secondly, phosphorylcarbenes readily undergo rearrangements; hydride, alkyl, aryl, or acyl shifts lead to phosphorylated alkenes. The phosphorylcarbene/methylenephosphane oxide rearrangement provides access to the short-lived P analogs of the ketenes. Finally, the vinylcarbene/allene rearrangement was first discovered in this connection; it competes with ring closure to the cyclopropene.
    Zusätzliches Material: 11 Tab.
    Materialart: Digitale Medien
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  • 28
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 14 (1975), S. 734-745 
    ISSN: 0570-0833
    Schlagwort(e): Substitution ; Radical ions ; Intermediates ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A new type of substition process at a saturated carbon atom is described. These reactions, which proceed via a chain sequence in which radical anions and free radicals are intermediates, are noteworthy for providing novel and powerful means of synthesis: they occur readily under mild conditions, they give excellent yields of pure products, and, in contrast to SN2 displacements, they are rather insensitive to steric hindrance. As a consequence, radical anion processes are especially valuable for the preparation of highly branched structures. Many inorganic and organic anions readily enter into these displacements and, indeed, amines are also effective. Systems which undergo substitutions via this electron transfer mechanism include benzylic, cumylic, strictly aliphatic, and heterocyclic molecules. It is of interest that a number of groups which do not behave as leaving groups in SN2 displacements are readily displaced at room temperature from a satureted carbon atom via the radical anion-free radical pathway, e.g., nitro, azide, sulfone, and ether groups.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
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  • 29
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 14 (1975), S. 801-811 
    ISSN: 0570-0833
    Schlagwort(e): Tetrachloromethane ; Phosphanes ; Chlorination ; Dehydration ; Synthetic methods ; Phosphorus-nitrogen compounds ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: In this review the processes occurring on the treatment of triphenylphosphane with tetrachloromethane are first reported; a key role is played here by (trichloromethyl)phosphonium chloride which reacts with a further amount of the phosphane to give the stable salt [chloro(triphenylphos-phoranediyl)methyl]triphenylphosphonium chloride by way of dichlorophosphorane and (dichloromethylene)phosphorane that is detectable only as an intermediate. The preparative application of the two-component system as a chlorinating, dehydrating, and P - N-linking reagent is ascribable to “phosphorylation”Here and below, “phosphorylation” is used lo mean in general the formation of a phosphorus derivative. In the narrower sense this term denotes the introduction of phosphoryl groups P(O). of the substrate in question through several reactive species. In these applications the reactions with the substrate compete with reactions of the two-component system with itself, so that the overall course of the reaction is in nearly all cases much more complex than was previously assumed. Nevertheless. very good results can be achieved by the use of this reagent, high yields and mild reaction conditions being characteristic.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 30
    ISSN: 0570-0833
    Schlagwort(e): Halomalondialdehydes ; Malondialdehydes ; Synthetic methods ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The present progress report provides a survey of the synthesis, structure, and reactions of halomalondialdehydes, including “cyanomalondialdehyde” (diformylacetonitrile), the only pseudohalogen compound so far known in this series. Halomalondialdehydes are reactive compounds, applicable in a variety of ways, and are characterized particularly by their cyclizations with bifunctional compounds. Many of the reactions discussed below can be applied to substituted malondialdehydes other than those specified.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 31
    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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  • 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): 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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  • 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
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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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