Issue 36, 2013

Asymmetric synthesis of α-alkenyl homoallylic primary aminesvia1,2-addition of Grignard reagent to α,β-unsaturated phosphonyl imines

Abstract

A series of chiral N-phosphonyl protected α-alkenyl homoallylic primary amines were synthesized by asymmetric addition of allylmagnesium bromide to chiral α,β-unsaturated imines. Only the 1,2-adduct was obtained for all the imines with good yields and excellent diastereoselectivities. The chiral auxiliary could be easily removed under simple conditions, giving free multiple functionalized primary amines.

Graphical abstract: Asymmetric synthesis of α-alkenyl homoallylic primary amines via 1,2-addition of Grignard reagent to α,β-unsaturated phosphonyl imines

Supplementary files

Article information

Article type
Paper
Submitted
30 Apr 2013
Accepted
26 Jun 2013
First published
26 Jun 2013

RSC Adv., 2013,3, 15820-15826

Asymmetric synthesis of α-alkenyl homoallylic primary amines via 1,2-addition of Grignard reagent to α,β-unsaturated phosphonyl imines

Y. Xiong, H. Mei, C. Xie, J. Han, G. Li and Y. Pan, RSC Adv., 2013, 3, 15820 DOI: 10.1039/C3RA42927J

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