Halides-based electrophiles mediated epoxide ring-opening reactions of α,β-epoxysulfoxides in C6-series : Deoxygenation versus dehydration and an overall 1,2-keto transposition-Reference-Cited by-同舟云学术

Halides-based electrophiles mediated epoxide ring-opening reactions of α,β-epoxysulfoxides in C6-series : Deoxygenation versus dehydration and an overall 1,2-keto transposition

Published:1994-05 Issue:18 Volume:50 Page:5413-5424
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Barillier Daniel,Levillain Jocelyne,Vazeux Michel

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference64 articles.

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5. Branching strategy in organic synthesis. A versatile ketone to enone homologation

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2. ChemInform Abstract: Halide Based Electrophiles Mediated Epoxide Ring-Opening Reactions of . alpha.,β-Epoxysulfoxides in C6-Series: Deoxygenation versus Dehydration and an Overall 1,2-Keto Transposition.;ChemInform;2010-08-19

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4. Novel Synthesis of α-Amino Carboxamides and Their Related Compounds via α-Oxo Sulfones Starting from 2,2-Disulfonyloxiranes;Bulletin of the Chemical Society of Japan;2004-10

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