Remarkably Mild and Simple Preparation of Sulfenate Anions from β-Sulfinylesters: A New Route to Enantioenriched Sulfoxides-Reference-Cited by-同舟云学术

Remarkably Mild and Simple Preparation of Sulfenate Anions from β-Sulfinylesters: A New Route to Enantioenriched Sulfoxides

Published:2005-02-22 Issue:7 Volume:70 Page:2812-2815
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Caupène Caroline¹,Boudou Cédric¹,Perrio Stéphane¹,Metzner Patrick¹

Affiliation:

1. Laboratoire de Chimie Moléculaire et Thio-organique (UMR CNRS 6507), ENSICaen−Université de Caen Basse−Normandie, 6 Boulevard du Maréchal Juin, 14050 Caen, France stephane.perrio@ensicaen.fr

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0478003

Reference30 articles.

1. Generation, structure and reactions of sulfenic acid anions

2. Oxaziridine-Mediated Oxidation Reaction of Thiolates To Give Sulfenates: The First One-Pot Synthesis of Sulfoxides from Thiols

3. Novel Approach to the Synthesis of Enantioenriched Sulfoxides. Highly Diastereoselective Alkylation of Sulfenate Anions with 1,4-Asymmetric Induction

4. Highly Chemoselective Oxidation of Dithioester Enethiolates to Sulfenates: Application to the Synthesis of Ketene Dithioacetal S-Oxides

5. A New Reaction of 2-(Phenylsulfonyl)-3-phenyloxaziridine (Davis Reagent): Oxidation of Thiolates to Sulfinates. Application to the Synthesis of Sulfones

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