The compatibility of the cyano and alkyl chloride functions in phenylthioalkylation reactions of O-silylated enolates
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. Selective reaction of silyl enol ethers with α-chloro-sulphides containing a ketone group
2. Dicétones-1,4 thiosubstituées
3. A regiospecific synthesis of γ-keto esters: the alkylation of o-silylated enolates with methyl α-chloro- α-phenylthioacetate
4. The methoxycarbonylalkylation and methoxycarbonylalkylidenation of silyl enol ethers
5. O-silylated enolate phenylthioalkylation: a new synthesis of unsaturated 1,5-dicarbonyl compounds.
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4. α-(Benzotriazolyl)methyl phenyl thioethers: Convenient reagents for α-phenylthioalkylation of silylated nucleophiles;Tetrahedron Letters;1996-09
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