Direct Lewis Acid Catalyzed Conversion of Enantioenriched N-Acyloxazolidinones to Chiral Esters, Amides, and Acids-Reference-Cited by-同舟云学术

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

Published:2018-11-09 Issue:23 Volume:83 Page:14245-14261
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Stevens Jason M.¹^ORCID,Parra-Rivera Ana Cristina²,Dixon Darryl D.¹,Beutner Gregory L.¹^ORCID,DelMonte Albert J.¹^ORCID,Frantz Doug E.²^ORCID,Janey Jacob M.¹,Paulson James¹,Talley Michael R.¹

Affiliation:

1. Chemical and Synthetic Development, Bristol-Myers Squibb, 1 Squibb Drive, New Brunswick, New Jersey 08901, United States

2. Department of Chemistry, The University of Texas at San Antonio, San Antonio, Texas 78249, United States

Funder

Division of Chemistry

Max and Minnie Tomerlin Voelcker Fund

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b02451

Reference82 articles.

1. Asymmetric alkylation reactions of chiral imide enolates. A practical approach to the enantioselective synthesis of .alpha.-substituted carboxylic acid derivatives

2. Diastereoselective Alkylations of Oxazolidinone Glycolates: A Useful Extension of the Evans Asymmetric Alkylation

3. Acyclic Stereocontrol in Radical Reactions:ρ-Selectivity with Oxazolidinone Auxiliories

4. 1,2-Amino Alcohols and Their Heterocyclic Derivatives as Chiral Auxiliaries in Asymmetric Synthesis

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