Issue 7, 2000

The synthesis of 2-trialkylsilylaziridines from vinyltrialkylsilanes or the reaction of α-chloro-α-silyl carbanions with imines

Abstract

Three methods have been employed in the synthesis of 2-trialkylsilylaziridines. Firstly, reacting α-chloro-α-silyl carbanions with imines. Secondly, from the corresponding vinylsilane, via addition of bromoazide to give the 1-bromo-2-azide, followed by reduction. Finally, by the addition of organoazides to vinylsilanes using thermochemical and photochemical conditions. Using these three strategies a range of substitution patterns have been achieved.

Article information

Article type
Paper
Submitted
28 Jun 1999
Accepted
03 Feb 2000
First published
24 Mar 2000

J. Chem. Soc., Perkin Trans. 1, 2000, 1173-1180

The synthesis of 2-trialkylsilylaziridines from vinyltrialkylsilanes or the reaction of α-chloro-α-silyl carbanions with imines

A. R. Bassindale, P. A. Kyle, M. Soobramanien and P. G. Taylor, J. Chem. Soc., Perkin Trans. 1, 2000, 1173 DOI: 10.1039/A905182A

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