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Digitale Medien

The Biosynthesis of Alkaloids IIPart I of this review appeared in Angew. Chem. Internet. Edit. 2, 341 (1963). (1963)

Mothes, K. ; Schütte, H. R.

Weinheim : Wiley-Blackwell

Angewandte Chemie International Edition in English 2 (1963), S. 441-458

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ISSN: 0570-0833

Schlagwort(e): Biosynthesis ; Alkaloids ; Chemistry ; General Chemistry

Quelle: Wiley InterScience Backfile Collection 1832-2000

Thema: Chemie und Pharmazie

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1002/anie.196304411

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Kinetics and Mechanism of 1,3-Dipolr CycloadditionsExtended version of a lecture given at the Annual Meeting of the Dechema in Frankfurt/Main on June 14th, 1962, and of the Max Tishler Lecture at Harvard University on December 10th, 1962. (1963)

Huisgen, R.

Weinheim : Wiley-Blackwell

Angewandte Chemie International Edition in English 2 (1963), S. 633-645

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ISSN: 0570-0833

Schlagwort(e): Kinetics ; Dipolar cycloaddition ; Cycloaddition ; Heterocycles ; Reaction mechanisms ; Chemistry ; General Chemistry

Quelle: Wiley InterScience Backfile Collection 1832-2000

Thema: Chemie und Pharmazie

Notizen: Criteria for the mechanism of 1,3-dipolar cycloadditions which lead to 5-membered rings are provided by the stereoselectivity observed with cis-trans isomeric dipolarophiles, by the effect of solvent and substituents on the rate constants, by the activation parameters, and by orientation phenomena. A concerted addition, which can also be described in terms of molecular orbitals and in which the two new σ-bonds are formed simultaneously, although not necessarily at equal rates, offers the best explanation of the experimental facts.

Zusätzliches Material: 2 Ill.

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1002/anie.196306331

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The Biogenesis of Ergot AlkaloidsDedicated to Professor Hans von Euler on the occasion of his 90th birthday (1963)

Weygand, F. ; Floss, H.-G.

Weinheim : Wiley-Blackwell

Angewandte Chemie International Edition in English 2 (1963), S. 243-247

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ISSN: 0570-0833

Schlagwort(e): Ergot alkaloids ; Alkaloids ; Biosynthesis ; Chemistry ; General Chemistry

Quelle: Wiley InterScience Backfile Collection 1832-2000

Thema: Chemie und Pharmazie

Notizen: In this article the biogenesis of the ergoline ring in lysergic acid derivatives and the clavines is discussed. T·yptophan and mevalonic acid are the precursors. The N-methyl group is supplied by formate or methionine. Concepts and results dealing with the manner in which the compounds are formed are discussed. Finally, the known biogenetic relationships among the ergot alkaloids are discussed in connection with their biogenesis.

Zusätzliches Material: 1 Tab.

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1002/anie.196302431

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Syntheses of Heterocyclic Compounds from Aminoguanidine (1963)

Kurzer, F. ; Godfrey, L. E. A.

Weinheim : Wiley-Blackwell

Angewandte Chemie International Edition in English 2 (1963), S. 459-476

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ISSN: 0570-0833

Schlagwort(e): Aminoguanidine ; Heterocycles ; Chemistry ; General Chemistry

Quelle: Wiley InterScience Backfile Collection 1832-2000

Thema: Chemie und Pharmazie

Notizen: Due to its unique structure, aminoguanidine is capable of reacting as a derivative of hydrazine, guanidine or formamidine. Addition and condensation reactions yield products which can be cyclized to heterocyclic compounds. Frequently, heterocyclics are directly accessible from aminoguanidine in one stage.

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1002/anie.196304591

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1,3-Dipolar Cycloadditions. Past and FutureExtended version of lectures given at the Chemists' Meeting in Vienna (Austria) October 1961, and at the Gordon Research Conference, New Hampton (U.S.A.), 1961. (1963)

Huisgen, Rolf

Weinheim : Wiley-Blackwell

Angewandte Chemie International Edition in English 2 (1963), S. 565-598

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ISSN: 0570-0833

Schlagwort(e): Dipolar cycloaddition ; Cycloaddition ; Heterocycles ; Chemistry ; General Chemistry

Quelle: Wiley InterScience Backfile Collection 1832-2000

Thema: Chemie und Pharmazie

Notizen: In contrast to the very large number of special methods applicable to syntheses in the heterocyclic series, relatively few general methods are available. The 1,3-dipolar addition offers a remarkably wide range of utility in the synthesis of five-membered heterocycles. Here the “1,3-dipole”, which can only be represented by zwitterionic octet resonance structures, combines in a cycloaddition with a multiple bond system - the “dipolarophile” - to form an uncharged five-membered ring. Although numerous individual examples of this reaction were known, some even back in the nineteenth century, fruitful development of this synthetic principle has been achieved only in recent years.

Zusätzliches Material: 4 Tab.

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1002/anie.196305651

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The Biosynthesis of Alkaloids IPart II of this review will appear in a subsequent issue of this journal.Dedicated to Professor Dr. Adolf Butenandt on the occasion of his 60th birthday (1963)

Mothes, K. ; Schütte, H. R.

Weinheim : Wiley-Blackwell

Angewandte Chemie International Edition in English 2 (1963), S. 341-357

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ISSN: 0570-0833

Schlagwort(e): Biosynthesis ; Alkaloids ; Chemistry ; General Chemistry

Quelle: Wiley InterScience Backfile Collection 1832-2000

Thema: Chemie und Pharmazie

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1002/anie.196303411

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