Diastereoselective routes to a 1.beta.-methylcarbapenem key intermediate. Scope of ate complex formation between ester enolates and organoboranes and -alanes-Reference-Cited by-同舟云学术

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Diastereoselective routes to a 1.beta.-methylcarbapenem key intermediate. Scope of ate complex formation between ester enolates and organoboranes and -alanes

Published:1992-04 Issue:8 Volume:57 Page:2411-2418
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Bender Dean R.,DeMarco Anthony M.,Melillo David G.,Riseman Stephen M.,Shinkai Ichiro

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo00034a039

Cited by 23 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. Formation of Nitriles, Carboxylic Acids, and Derivatives by Alkylation, Acylation, and Substitution;Comprehensive Organic Transformations;2018-02-28

2. ChemInform Abstract: Diastereoselective Routes to a 1β-Methylcarbapenem Key Intermediate. Scope of Ate Complex Formation Between Ester Enolates and Organoboranes and -alanes.;ChemInform;2010-08-21

3. Triethylborane;Encyclopedia of Reagents for Organic Synthesis;2007-03-15

4. Triethylborane-Triethylaluminum;Fieser and Fieser's Reagents for Organic Synthesis;2006-12-15

5. Asymmetric synthesis of β-amino acids and β-lactam derivatives via conjugate addition of metal amides;Advances in Asymmetric Synthesis Volume 3;1999

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