Issue 39, 2017

Ligand-free nickel-catalyzed semihydrogenation of alkynes with sodium borohydride: a highly efficient and selective process for cis-alkenes under ambient conditions

Abstract

We report a low-cost and efficient catalytic system, involving in situ generated ligand-free Ni NPs, methanol and sodium borohydride, for the semihydrogenation of alkynes under ambient conditions. This catalytic system exhibits remarkably high activity, satisfactory cis-selectivity for internal alkynes, good stability and general applicability.

Graphical abstract: Ligand-free nickel-catalyzed semihydrogenation of alkynes with sodium borohydride: a highly efficient and selective process for cis-alkenes under ambient conditions

Supplementary files

Article information

Article type
Communication
Submitted
21 Mar 2017
Accepted
05 Apr 2017
First published
05 Apr 2017

Chem. Commun., 2017,53, 5372-5375

Ligand-free nickel-catalyzed semihydrogenation of alkynes with sodium borohydride: a highly efficient and selective process for cis-alkenes under ambient conditions

X. Wen, X. Shi, X. Qiao, Z. Wu and G. Bai, Chem. Commun., 2017, 53, 5372 DOI: 10.1039/C7CC02140B

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