Additive Pummerer reactions of vinylic sulfoxides. Synthesis of γ-hydroxy-α,β-unsaturated esters, α-hydroxyketones, and 2-phenylsulfenyl aldehydes and primary alcohols-Reference-Cited by-同舟云学术

Additive Pummerer reactions of vinylic sulfoxides. Synthesis of γ-hydroxy-α,β-unsaturated esters, α-hydroxyketones, and 2-phenylsulfenyl aldehydes and primary alcohols

Published:1993-01 Issue:48 Volume:49 Page:11263-11304
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Craig Donald,Daniels Kevin,MacKenzie A.Roderick

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference55 articles.

1. Pummerer-type reaction of 2-benzylidene-2,3-dihydro-5-methylbenzo[b]-thiophen-3-one 1-oxide

2. A Novel Rearrangement of Styryl Sulfoxide Induced by Phosphorus Pentachloride

3. The regiospecific Pummerer-like introduction of chlorine atoms into pyrrol-3-yl and indol-3-yl sulfoxides

4. Additive Pummerer rearrangement of methyl cyclopentylidene(phenylsulphinyl)-acetate induced by acetyl chloride, trifluoroacetic anhydride, or thionyl chloride

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