Kinetic Resolution of β-Sulfonyl Ketones through Enantioselective β-Elimination using a Cation-Binding Polyether Catalyst-Reference-Cited by-同舟云学术

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Kinetic Resolution of β-Sulfonyl Ketones through Enantioselective β-Elimination using a Cation-Binding Polyether Catalyst

Published:2015-11-18 Issue:1 Volume:55 Page:331-335
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Li Liang,Liu Yidong,Peng Yang,Yu Lei,Wu Xiaoyan,Yan Hailong

Funder

Fundamental Research Funds for the Central Universities

100 Young Plan by Chongqing University

NSFC

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference92 articles.

1. The Volume of Activation in Elimination Reactions

2. Some aspects of organosulfur-mediated synthetic methods

3. Leaving groups and nucleofugality in elimination and other organic reactions

4. Substitution and Elimination ReactionsviaOne Electron Transfer Process. A New Olefin Synthesis from β-Nitro Sulfones

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1. Asymmetric Sulfonylation from a Reaction of Cyclopropan-1-ol, Sulfur Dioxide, and 1-(Alkynyl)naphthalen-2-ol;Organic Letters;2024-04-10

2. Enantioselective Sulfonation of Enones with Sulfinates by Thiourea/Tertiary-Amine Catalysis;Synlett;2023-10-31

3. Photocatalytic Enantioselective Hydrosulfonylation of α,β‐Unsaturated Carbonyls with Sulfonyl Chlorides;Angewandte Chemie International Edition;2023-10-13

4. Photocatalytic Enantioselective Hydrosulfonylation of α,β‐Unsaturated Carbonyls with Sulfonyl Chlorides;Angewandte Chemie;2023-10-13

5. Rh-Catalyzed Asymmetric Hydrogenation of α-Substituted Alkenyl Sulfones: Highly Chemo- and Enantioselective Access to Chiral Sulfones;Organic Letters;2023-09-13

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