Convenient stereoselective synthesis of 3-hydroxy-2-iodo-2(E)-alkenyl sulfides via iodohydroxylation of 1,2-allenyl sulfoxides in the presence of BnSH-Reference-Cited by-同舟云学术

Convenient stereoselective synthesis of 3-hydroxy-2-iodo-2(E)-alkenyl sulfides via iodohydroxylation of 1,2-allenyl sulfoxides in the presence of BnSH

Published:2004-07 Issue:31 Volume:45 Page:6063-6065
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Fu Chunling,Huang Xian,Ma Shengming

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference11 articles.

1. Hydrohalogenation Reaction of 1,2-Allenic Sulfoxides with AlX3 and H2O: Efficient Synthesis of 2-Haloallyl Sulfoxides

2. An Efficient New Methodology for the Synthesis of 1-Functionalized 2-Halo-2-alkenes via Hydrohalogenation Reaction of Electron-Deficient Allenes

3. Unique Selectivity of Iodohydroxylation Reaction of Allenyl Phenyl Sulfoxides in Aqueous MeCN. A Stereodefined Synthesis of (E)-2-Iodo-3-hydroxy-1-alkenyl Sulfoxides

4. Highly Regio- and Stereoselective Halohydroxylation Reaction of 1,2-Allenyl Phenyl Sulfoxides. Reaction Scope, Mechanism, and the Corresponding Pd- or Ni-Catalyzed Selective Coupling Reactions

5. Reversed Stereoselectivity in Iodohydroxylation of Allenyl Sulfides. An Efficient Synthesis of (Z)-3-Organosulfur-2-iodo-2-propenols

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