The Nitrile Functionality as a Directing Group in the Palladium-Catalysed Addition of Aryl Boronic Acids to Alkynes

Arantxa      Rodriguez; Wesley   J.   Moran

doi:10.2174/157017810790533931

Author(s): Arantxa Rodriguez and Wesley J. Moran

Volume 7, Issue 1, 2010

Page: [7 - 10] Pages: 4

DOI: 10.2174/157017810790533931

Price: $65

Abstract

The nitrile group is shown to direct the palladium-catalysed hydroarylation of internal alkynes bearing a pendant nitrile with boronic acids.

Keywords: Palladium, catalysis, nitrile, directing-group, hydroarylation

« Previous Next »

Rights & Permissions Print Cite

Letters in Organic Chemistry

Title: The Nitrile Functionality as a Directing Group in the Palladium-Catalysed Addition of Aryl Boronic Acids to Alkynes

Volume: 7 Issue: 1

Author(s): Arantxa Rodriguez and Wesley J. Moran

Affiliation:

Keywords: Palladium, catalysis, nitrile, directing-group, hydroarylation

Abstract: The nitrile group is shown to direct the palladium-catalysed hydroarylation of internal alkynes bearing a pendant nitrile with boronic acids.

Export Options

Export File:

RIS (for EndNote, Reference Manager, ProCite)

BibTeX

Text

Content:

Citation Only

Citation and Abstract

About this article

Cite this article as:

Rodriguez Arantxa and Moran J. Wesley, The Nitrile Functionality as a Directing Group in the Palladium-Catalysed Addition of Aryl Boronic Acids to Alkynes, Letters in Organic Chemistry 2010; 7 (1) . https://dx.doi.org/10.2174/157017810790533931