Enantio- and Diastereoselective Synthesis of Homopropargyl Amines by Copper-Catalyzed Coupling of Imines, 1,3-Enynes, and Diborons

39Citations
Citations of this article
21Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

An efficient, enantio- and diastereoselective, copper-catalyzed coupling of imines, 1,3-enynes, and diborons is reported. The process shows broad substrate scope and delivers complex, chiral homopropargyl amines; useful building blocks on the way to biologically-relevant compounds. In particular, functionalized homopropargyl amines bearing up to three contiguous stereocenters can be prepared in a single step.

Cite

CITATION STYLE

APA

Manna, S., Dherbassy, Q., Perry, G. J. P., & Procter, D. J. (2020). Enantio- and Diastereoselective Synthesis of Homopropargyl Amines by Copper-Catalyzed Coupling of Imines, 1,3-Enynes, and Diborons. Angewandte Chemie - International Edition, 59(12), 4879–4882. https://doi.org/10.1002/anie.201915191

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