1-Methoxy-1-(phenylthio)cyclopropanes from olefins via the Pummerer rearrangement
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 articles.
1. A practical method for using alkoxide-accelerated vinylcyclobutane ring expansions in the synthesis of six-membered rings. Unexpected orbital symmetry allowed and forbidden 1,3-sigmatropic rearrangements
2. An unusual migratory aptitude in a cyclopropylcarbinyl-cyclobutyl rearrangement. Synthesis of 2,4-disubstituted cyclobutanones
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1. A novel synthetic method for alkylidenecyclopropanes based on the reaction of magnesium cyclopropylidenes with lithium α-sulfonyl carbanions;Tetrahedron Letters;2004-01
2. Magnesium Amide-Induced Pummerer-Type Reactions of Cyclopropyl Sulfoxides. Synthesis of Cyclopropanone Dithioacetals;Bulletin of the Chemical Society of Japan;2002-06
3. Magnesium cyclopropylidenes generated from 1-chlorocyclopropyl phenyl sulfoxides with Grignard reagents: their properties, and a sulfoxide version of the Doering–Moore–Skattebol reaction;Tetrahedron;2001-06
4. Phenylthiocyclopropanea,c;Encyclopedia of Reagents for Organic Synthesis;2001-04-15
5. Chloromethyl Phenyl Sulfide;Encyclopedia of Reagents for Organic Synthesis;2001-04-15
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