Issue 24, 2006

The first catalytic Sakurai reaction of N-alkoxycarbonylamino sulfones with allyltrimethylsilane

Abstract

We report the first catalytic Sakurai reaction of N-alkoxycarbonylamino sulfones with allylsilanes. The allylation reaction of N-alkoxycarbonylamino phenylsulfones with allyltrimethylsilane proceeded smoothly with low catalyst loading of bismuth triflate (2.0 mol%) to afford the corresponding protected homoallylic amines in moderate to very good yields (up to 96%).

Graphical abstract: The first catalytic Sakurai reaction of N-alkoxycarbonylamino sulfones with allyltrimethylsilane

Article information

Article type
Communication
Submitted
18 Sep 2006
Accepted
31 Oct 2006
First published
10 Nov 2006

Org. Biomol. Chem., 2006,4, 4440-4443

The first catalytic Sakurai reaction of N-alkoxycarbonylamino sulfones with allyltrimethylsilane

T. Ollevier and Z. Li, Org. Biomol. Chem., 2006, 4, 4440 DOI: 10.1039/B613331B

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