Enantioselective synthesis of (1 S ,4 R )- N -(benzylcarbamoyl)-4-aminocyclopent-2-en-1-ol by Candida antarctica lipase B-Reference-Cited by-同舟云学术

Enantioselective synthesis of (1 S ,4 R )- N -(benzylcarbamoyl)-4-aminocyclopent-2-en-1-ol by Candida antarctica lipase B

Published:2015-11 Issue:11 Volume:26 Page:1431-1434
ISSN:1001-8417
Container-title:Chinese Chemical Letters
language:en
Short-container-title:Chinese Chemical Letters

Author:

Wen Hui-Jiao,Chen Qing,Zheng Guo-Jun

Funder

Fundamental Research Funds for the Central Universities

Publisher

Elsevier BV

Subject

General Chemistry

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4. Synthesis of 4′-modified noraristeromycins to clarify the effect of the 4′-hydroxyl groups for inhibitory activity against S-adenosyl-l-homocysteine hydrolase;Ando;Bioorg. Med. Chem. Lett.,2008

5. Enantioselective synthesis of 4-acetylaminocyclopent-2-en-1-ols from tricyclo[5.2.1.0(2, 6)]decenyl enaminones. Precursors for 5′-norcarbocyclic nucleosides and related antiviral compounds;Ramesh;J. Org. Chem.,1999

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