Issue 10, 2015

Enantioselective nickel-catalyzed alkylative alkyne–aldehyde cross-couplings

Abstract

An efficient asymmetric nickel-catalyzed alkylative alkyne–aldehyde cross-coupling is developed by employing a P-chiral monophosphorus ligand BI-DIME, allowing rapid access to a series of chiral tetra-substituted olefinic allylic alcohols in high yields and good to excellent ees. The three-component reactions enjoy excellent regio- and enantioselectivities, and a broad substrate scope from readily available starting materials.

Graphical abstract: Enantioselective nickel-catalyzed alkylative alkyne–aldehyde cross-couplings

Supplementary files

Article information

Article type
Research Article
Submitted
04 máj 2015
Accepted
22 júl 2015
First published
23 júl 2015

Org. Chem. Front., 2015,2, 1322-1325

Enantioselective nickel-catalyzed alkylative alkyne–aldehyde cross-couplings

M. Nie, W. Fu, Z. Cao and W. Tang, Org. Chem. Front., 2015, 2, 1322 DOI: 10.1039/C5QO00148J

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements