Asymmetric Carbon-Carbon Bond Formations by the Reaction of “Chiral Episulfonium Ions” with Enol Silyl Ethers
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/21/2/21_2_239/_pdf
Reference10 articles.
1. Enantioselectivity in the ritter-type substitution reaction via qpisulfonium ion: Retention of configuration
2. Reaction of silyl enol ethers with β-halogenoalkyl aryl sulfides - a method of β-arylthioalkylation of carbonyl compounds
3. O-silylated enolates in organic synthesis: sulphur-mediated alkylation of esters with alkenes.
4. Alkene carbosulphenylation and carboselenylation: The use of allyltrimethylsilane and o-silylated enolates.
5. A highly regioselective reaction of allylic acetates with silylated carbon nucleophiles directed by a sulfenyl group
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1. Catalytic, Enantioselective, Intramolecular Carbosulfenylation of Olefins. Preparative and Stereochemical Aspects;The Journal of Organic Chemistry;2013-12-11
2. Catalytic, Enantioselective, Intramolecular Carbosulfenylation of Olefins;Journal of the American Chemical Society;2013-04-19
3. ChemInform Abstract: Asymmetric Carbon-Carbon Bond Formations by the Reaction of “Chiral Episulfonium Ions” with Enol Silyl Ethers.;ChemInform;2010-09-01
4. Highly stereoselective Friedel–Crafts alkylations of unactivated benzenes by episulfonium ion cyclizations;Tetrahedron Letters;2002-01
5. Further Characterization of Galloyl Pedunculagin as an Effective Autophosphorylation Inhibitor of C-Kinase in Vitro.;Biological and Pharmaceutical Bulletin;2002
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