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Radical cyclization of β-allenic oxime ethers

Authors
Journal
Tetrahedron Letters
0040-4039
Publisher
Elsevier
Publication Date
Volume
33
Issue
8
Identifiers
DOI: 10.1016/s0040-4039(00)91859-8

Abstract

Abstract β-allenic O-methyl oximes undergo a free radical hydrostannylation reaction to afford cyclopentenes bearing a protected amine group and a vinyl stannyl fonction. These compounds were destannylated to yield the corresponding cyclopentenes.

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