Regio- and stereoselective carbometallation reactions of N-alkynylamides and sulfonamides

48Citations
Citations of this article
17Readers
Mendeley users who have this article in their library.

Abstract

The carbocupration reactions of heterosubstituted alkynes allow the regio- and stereoselective formation of vinyl organometallic species. N-Alkynylamides (ynamides) are particularly useful substrates for the highly regioselective carbocupration reaction, as they lead to the stereodefined formation of vinylcopper species geminated to the amide moiety. The latter species are involved in numerous synthetically useful transformations leading to valuable building blocks in organic synthesis. Here we describe in full the results of our studies related to the carbometallation reactions of N-alkynylamides. © 2013 Minko et al.

Cite

CITATION STYLE

APA

Minko, Y., Pasco, M., Chechik, H., & Marek, I. (2013). Regio- and stereoselective carbometallation reactions of N-alkynylamides and sulfonamides. Beilstein Journal of Organic Chemistry, 9, 526–532. https://doi.org/10.3762/bjoc.9.57

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