On the favorskii rearrangememt of dichloromethylketones.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. Halogen Substituted 1,3-Cyclohexanediones I. Reaction of 2,2-dichlorodimedone with bases
2. Halogen Substituted 1,3-Cyclohexanediones II. New Chlorinated Cycloalkanones from 2, 2-Dichlorodimedone
3. Schamp, N.; Bull. Soc. Chim. Belges, in press.
4. Favorsky Rearrangements. I. A New Synthesis of Isocrotonic Acid.
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1. Chemoselective Reduction: Xanthates as Traceless Precursors of Polyfunctionalized α,α-Dichloroketones;Organic Letters;2017-10-05
2. Radical Solution to the Alkylation of the Highly Base-Sensitive 1,1-Dichloroacetone. Application to the Synthesis of Z-Alkenoates and E,E-Dienoates;Organic Letters;2015-10-12
3. Reactivity of N-2-(1,1-Dichloroalkylidene) Cyclohexylamines. II;Bulletin des Sociétés Chimiques Belges;2010-09-02
4. A New Synthesis of 1,1-Dichloromethylketones;Bulletin des Sociétés Chimiques Belges;2010-09-02
5. Favorskii rearrangement of a highly functionalized meso-dihaloketone;Tetrahedron: Asymmetry;2009-05
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