Nickel/AlMe2Cl-catalysed carbocyanation of alkynes using arylacetonitriles

Akira Yada; Tomoya Yukawa; Yoshiaki Nakao; Tamejiro Hiyama

doi:10.1039/B907290J

skip RSC | ChemSpider | Feedback

Home > Journals > Chemical Communications > Nickel/AlMe2Cl-catalyse...

Authors & Referees | Librarians

You do not have JavaScript enabled. Please enable JavaScript to access the full features of the site or access our non-JavaScript page.

Chemical Communications

Issue 26, 2009

More about this Journal
Editorial Board
Submit an Article

Follow Journal | |

Journal Home | RSC Journals

Communication

Previous Article | Next Article

Nickel/AlMe₂Cl-catalysed carbocyanation of alkynes using arylacetonitriles

Akira Yada , Tomoya Yukawa , Yoshiaki Nakao and Tamejiro Hiyama

Chem. Commun., 2009, 3931-3933

DOI: 10.1039/B907290J
Received 14 Apr 2009, Accepted 05 May 2009
First published on the web 26 May 2009
This article is part of the collection: Selective Catalysis for Organic Synthesis

Please wait while Download options loads

Request Permissions

Abstract
Cited by
Compounds
Related Content

Nickel/Lewis acid dual catalysis was found to effect the carbocyanation reaction of alkynes using arylacetonitriles, giving a range of triply substituted acrylonitriles; the reaction of optically active α-phenylpropionitrile suggested a reaction mechanism that involves oxidative addition of a C–CN bond with retention of its absolute configuration.

Abstract from Catalysts & Catalysed Reactions 2009

No abstract available

Abstract from Methods in Organic Synthesis 2009

No abstract available

This may take some time to load.

Supplementary Info

General experimental information, spectral data andcrystallographic data for the structure of (Z)-3ac
PDF (994K)
Crystal structure data
TXT (15K)

Terms & Conditions|Privacy |Accessibility|ACAP Enabled

Chemical Communications

Nickel/AlMe₂Cl-catalysed carbocyanation of alkynes using arylacetonitriles

Log in (Free Access)

Log in (Subscriber Access)

Supplementary Info

Articles By