Issue 44, 2017

Highly efficient synthesis of unsymmetrical 1,3-diynes from organoalane reagents and alkynyl bromides mediated by a nickel catalyst

Abstract

Highly efficient and simple cross-coupling reactions of alkynylbromides with organoalane reagents for the synthesis of unsymmetrical 1,3-diynes derivatives using Ni(OAc)2 (2–5 mol%)/(o-furyl)3P (4–10 mol%) as a catalyst are reported. Excellent yields (up to 94%) were obtained for a wide range of substrates at rt or 60 °C for 2–3 h in Et2O or toluene.

Graphical abstract: Highly efficient synthesis of unsymmetrical 1,3-diynes from organoalane reagents and alkynyl bromides mediated by a nickel catalyst

Supplementary files

Article information

Article type
Paper
Submitted
07 Mar 2017
Accepted
18 May 2017
First published
23 May 2017
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2017,7, 27243-27247

Highly efficient synthesis of unsymmetrical 1,3-diynes from organoalane reagents and alkynyl bromides mediated by a nickel catalyst

S. Mo, X. Shao, G. Zhang and Q. Li, RSC Adv., 2017, 7, 27243 DOI: 10.1039/C7RA02758C

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