Diastereoselective Reaction of a Grignard Reagent with Chiral Imides: A Practical Preparation of a Key Intermediate in the Synthesis of Ifetroban Sodium-Reference-Cited by-同舟云学术

Diastereoselective Reaction of a Grignard Reagent with Chiral Imides: A Practical Preparation of a Key Intermediate in the Synthesis of Ifetroban Sodium

Published:1997-01-01 Issue:1 Volume:1 Page:14-19
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Mueller Richard H.¹,Wang Shaopeng¹,Pansegrau Paul D.¹,Jannotti Joy Q.¹,Poss Michael A.¹,Thottathil John K.¹,Singh Janak¹,Humora Michael J.¹,Kissick Thomas P.¹,Boyhan Brenda¹

Affiliation:

1. Chemical Process Research Department, The Bristol-Myers Squibb Pharmaceutical Research Institute, P.O. Box 4000, Princeton, New Jersey 08543-4000, and P.O. Box 191, New Brunswick, New Jersey 08903-0191

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/op960034k

Reference9 articles.

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3. Cupric bromide mediated oxidation of 4-carboxyoxazolines to the corresponding oxazoles

4. A novel and highly efficient desymmetrization of a meso-anhydride by a chiral grignard reagent

5. Some isoindolo-fused heterocyclic systems by cyclodehydration of N-arylalkyl-3-hydroxyphthalimidines

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