Ringöffnende Aminolyse von Lactamen, 2.5-(ω-Aminoalkyl)-1,2,4-oxadiazole aus Amidoximen und reaktiven Lactamen-Reference-Cited by-同舟云学术

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Ringöffnende Aminolyse von Lactamen, 2.5-(ω-Aminoalkyl)-1,2,4-oxadiazole aus Amidoximen und reaktiven Lactamen

Published:1978-05-11 Issue:2 Volume:1978 Page:306-311
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

Reference9 articles.

1. Liebigs Ann. Chem. (1976), 336.

2. Richardson-Merrell Inc. (Erf. und ) D. O. S. 2409262 (19. Sept. 1974)

3. Bayer AG (Erf. ), D. O. S. 2145513 (15. März 1973)

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Ring transformation with bridged 1,3-dicarbonyl heteroanalogues, III 5-(ω-aminoalkyl)-1,2,4-oxadiazoles by ring-transformations of 3-methylthio-2-aza-3-propeniminium salts;Archiv der Pharmazie;2010-08-25

2. Process Development of a Potent Bradykinin 1 Antagonist;Organic Process Research & Development;2009-03-06

3. Five-, Six-, and Seven-membered Lactim Ethers. Methods of Synthesis and Chemical Properties. (Review);Chemistry of Heterocyclic Compounds;2005-05

4. Volume 4 References;Comprehensive Heterocyclic Chemistry II;1996

5. 1,2,4-Oxadiazoles;Comprehensive Heterocyclic Chemistry II;1996

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