Efficient synthesis of β'-amino-α, β-unsaturated ketones

9Citations
Citations of this article
12Readers
Mendeley users who have this article in their library.

Abstract

A general and simple procedure to access chiral β'-amino-α, β-enones, in seven steps, from an α,β unsaturated ester has been described. The use of a Horner-Wadsworth-Emmons reaction as a key step for generating the β'-amino-α,β-enones, permits access to a range of substrates under mild conditions and in moderate to high yield. © 2013 Abrunhosa-Thomas et al.

Cite

CITATION STYLE

APA

Abrunhosa-Thomas, I., Plas, A., Kandepedu, N., Chalard, P., & Troin, Y. (2013). Efficient synthesis of β’-amino-α, β-unsaturated ketones. Beilstein Journal of Organic Chemistry, 9, 486–495. https://doi.org/10.3762/bjoc.9.52

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free