Issue 1, 1993

Michael addition of silylated telluronium allylide to α,β-unsaturated esters: facile and stereoselective synthesis of trimethylsilylvinylcyclopropane derivatives

Abstract

Trimethylsilylated diisobutyltelluronium allylide, generated from 3-trimethylsilylprop-2-enyldiisobutyltelluronium bromide 1 with lithium 2,2,6,6-tetramethylpiperidide (LTMP), reacts with α,β-unsaturated esters to afford trimethylsilylvinylcyclopropane derivatives via Michael addition in excellent yields with high stereoselectivity.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 7-9

Michael addition of silylated telluronium allylide to α,β-unsaturated esters: facile and stereoselective synthesis of trimethylsilylvinylcyclopropane derivatives

Y. Huang, Y. Tang, Z. Zhou and J. Huang, J. Chem. Soc., Chem. Commun., 1993, 7 DOI: 10.1039/C39930000007

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