Ringöffnende Aminolyse von Lactamen. Ein einfacher Zugang zu 2-(ω-aminoalkyl)substituierten, fünf-und sechsgliedrigen Heterocyclen-Reference-Cited by-同舟云学术

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Ringöffnende Aminolyse von Lactamen. Ein einfacher Zugang zu 2-(ω-aminoalkyl)substituierten, fünf-und sechsgliedrigen Heterocyclen

Published:1976-02-27 Issue:2 Volume:1976 Page:336-347
ISSN:0075-4617
Container-title:Justus Liebigs Annalen der Chemie
language:de
Short-container-title:Justus Liebigs Ann. Chem.

Author:

Botta Artur

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry,General Medicine

Reference23 articles.

1. Bayer AG (Erf. ), D. O. S. 837539 (28. April 1952),

2. Henkel & Cie. GmbH (Erf. und ), D. O. S. 2220016 (8. Nov. 1973)

3. Chemical Reactions of Caprolactam

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5. Synthesis of 2-(ω-aminoalkyl)imidazolin-4-ones by ring chain transformation of lactam derivatives with α-aminoamides;Journal of Heterocyclic Chemistry;1996-05

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