Cyanoalkylation: Alkylnitriles in Catalytic C-C Bond-Forming Reactions

Angew Chem Int Ed Engl. 2015 Nov 2;54(45):13170-84. doi: 10.1002/anie.201502493. Epub 2015 Sep 21.

Abstract

Alkylnitriles are one of the most ubiquitous nitrogen-containing chemicals and are widely employed in reactions which result in nitrile-group conversion into other functionalities. Nevertheless, their use as carbon pronucleophiles in carbon-carbon bond-forming reactions has been hampered by difficulties associated mainly with the catalytic generation of active species, that is, α-cyano carbanions or metalated nitriles. Recent investigations have addressed this challenge and have resulted in different modes of alkylnitrile activation. This review illustrates these findings, which have set the foundation for the development of practical and conceptually new catalytic, direct cyanoalkylation methodologies.

Keywords: alkylation; asymmetric catalysis; carbanions; nitriles; synthetic methods.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Alkylation
  • Catalysis
  • Molecular Structure
  • Nitriles / chemical synthesis*
  • Nitriles / chemistry*

Substances

  • Nitriles