Cerium(III) Chloride-Mediated Stereoselective Reduction of a 4-Substituted Cyclohexanone Using NaBH4-Reference-Cited by-同舟云学术

Cerium(III) Chloride-Mediated Stereoselective Reduction of a 4-Substituted Cyclohexanone Using NaBH4

Published:2019-12-03 Issue:12 Volume:23 Page:2754-2757
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Maity Prantik¹,Gujjar Manjunath¹,Vellingiri Raghukumar¹,Lakshminarasimhan Thirumalai¹,DelMonte Albert J.²^ORCID,Young Ian S.²^ORCID,Eastgate Martin D.²^ORCID,Vaidyanathan Rajappa¹^ORCID

Affiliation:

1. Chemical Development and API Supply, Biocon Bristol-Myers Squibb Research and Development Center, Biocon Park, Jigani Link Road, Bommasandra IV, Bangalore 560099, India

2. Chemical and Synthetic Development, Bristol-Myers Squibb Global Product Development and Supply, One Squibb Drive, P.O. Box 191, New Brunswick, New Jersey 08903-0191, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.oprd.9b00458

Reference31 articles.

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2. Direct Lewis Acid Catalyzed Conversion of Enantioenriched N-Acyloxazolidinones to Chiral Esters, Amides, and Acids

3. Rapid Development of a Commercial Process for Linrodostat, an Indoleamine 2,3-Dioxygenase (IDO) Inhibitor

4. Revisiting the Cleavage of Evans Oxazolidinones with LiOH/H2O2

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