Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5282061 | Tetrahedron Letters | 2009 | 6 Pages |
Abstract
Treatment of lithium ester enolates with magnesium alkylidene carbenoids, generated from 1-chlorovinyl p-tolyl sulfoxides with isopropylmagnesium chloride via the sulfoxide-magnesium exchange reaction, gave β,γ-unsaturated esters in moderate to good yields. When this reaction was conducted with the lithium ester enolates of α-chlorocarboxylic acid esters, allenic esters were obtained. This procedure provides an unprecedented way for the synthesis of β,γ-unsaturated esters and allenic esters from ketones with the construction of a carbon-carbon bond between α- and β-positions.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Tsuyoshi Satoh, Hiroaki Kaneta, Ayako Matsushima, Masanobu Yajima,