Development of a Practical, Safe, and High-Yielding Process for the Preparation of Enantiomerically Pure trans-Cyclopropane Carboxylic Acid-Reference-Cited by-同舟云学术

Development of a Practical, Safe, and High-Yielding Process for the Preparation of Enantiomerically Pure trans-Cyclopropane Carboxylic Acid

Published:2002-07-04 Issue:5 Volume:6 Page:618-620
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Singh Ambarish K.¹,Rao Meena N.¹,Simpson James H.¹,Li Wen-Sen¹,Thornton John E.¹,Kuehner Daniel E.¹,Kacsur David J.¹

Affiliation:

1. Process Research and Development, The Bristol-Myers Squibb Pharmaceutical Research Institute, One Squibb Drive, New Brunswick, New Jersey 08903-0191, U.S.A.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/op0202033

Reference14 articles.

1. Structure of Curacin A, a Novel Antimitotic, Antiproliferative and Brine Shrimp Toxic Natural Product from the Marine Cyanobacterium Lyngbya majuscula

2. Isolation and structure of constanolactones A and B, new cyclopropyl hydroxy-eicosanoids from the temperate red alga constantinea simplex

3. Copper(I)-catalyzed intramolecular cyclization reaction of 2-(2′-chlorophenyl)ethanol to give 2,3-dihydrobenzofuran

4. The Utility of Phosphonate Carbanions in Olefin Synthesis

5. A New Synthesis of Cyclopropanecarboxylic Acids

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