Asymmetric Synthesis of β-Mercapto Carboxylic Acid Derivatives by Intramolecular Sulfur Transfer in N-Enoyl Oxazolidine-2-thiones Promoted by Lewis Acids-Reference-Cited by-同舟云学术

Asymmetric Synthesis of β-Mercapto Carboxylic Acid Derivatives by Intramolecular Sulfur Transfer in N-Enoyl Oxazolidine-2-thiones Promoted by Lewis Acids

Published:2001-05-19 Issue:23 Volume:123 Page:5602-5603
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Palomo Claudio¹,Oiarbide Mikel¹,Dias Flavia¹,Ortiz Aurelio¹,Linden Anthony¹

Affiliation:

1. Departamento de Química Orgánica I Facultad de Química,Universidad del País Vasco Apdo. 1072, 20080 San Sebastián, Spain Organisch-chemisches Institut der Universität Zürich Winterthurerstrasse 190, CH-8057, Zürich, Switzerland

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja015860%2B

Reference19 articles.

1. Asymmetric Conjugate Addition of Thiols to Chiral .beta.-Substituted N-Enoylsultams

2. A Novel Tandem Michael Addition/Meerwein−Ponndorf−Verley Reduction: Asymmetric Reduction of Acyclic α,β-Unsaturated Ketones Using A Chiral Mercapto Alcohol

3. Alkaloid catalyzed asymmetric synthesis III the addition of mercaptans to 2-cyclohexene-1-one; determination of enantiomeric excess using 13C NMR.

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