Ring-Closing Metathesis-Based Synthesis of (3R,4R,5S)-4-Acetylamino-5-amino-3-hydroxy- cyclohex-1-ene-carboxylic Acid Ethyl Ester: A Functionalized Cycloalkene Skeleton of GS4104-Reference-Cited by-同舟云学术

Ring-Closing Metathesis-Based Synthesis of (3R,4R,5S)-4-Acetylamino-5-amino-3-hydroxy- cyclohex-1-ene-carboxylic Acid Ethyl Ester: A Functionalized Cycloalkene Skeleton of GS4104

Published:2006-06-06 Issue:14 Volume:71 Page:5365-5368
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Cong Xin¹,Yao Zhu-Jun¹

Affiliation:

1. State Key Laboratory of Bioorganic and Natural Product Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road, Shanghai 200032, China yaoz@mail.sioc.ac.cn

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo060633h

Reference26 articles.

1. Influenza Neuraminidase Inhibitors: Structure-Based Design of a Novel Inhibitor Series

2. Stereodivergent and Regioselective Synthesis of 3,4-cis- and 3,4-trans-Pyrrolidinediols from α-Amino Acids

3. Stereoselective Total Synthesis of Racemic BCX-1812 (RWJ-270201) for the Development of Neuraminidase Inhibitors as Anti-influenza Agents

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