Issue 22, 1994

First highly asymmetric Pummerer-type reaction in chiral, non-racemic acyclic sulfoxides induced by O-silylated ketene acetal

Abstract

Various types of syn- and anti-β-substituted sulfoxides 6be, g reacted with ketene tert-butyldimethylsilyl acetal 2 in the presence of a catalytic amount of zinc iodide in acetonitrile to give high yields of the corresponding α-siloxy sulfides 7be, g stereoselectively. Similarly, chiral, nonracemic sulfoxides 6a, f, h, i reacted with acetal 2 in acetonitrile to give the chiral, non-racemic α-siloxy sulfides 7a, f, h, i in high yields.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1994, 3335-3341

First highly asymmetric Pummerer-type reaction in chiral, non-racemic acyclic sulfoxides induced by O-silylated ketene acetal

Y. Kita, N. Shibata, N. Yoshida and S. Fujita, J. Chem. Soc., Perkin Trans. 1, 1994, 3335 DOI: 10.1039/P19940003335

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