4.8 Review

Cyanoalkylation: Alkylnitriles in Catalytic CC Bond-Forming Reactions

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 54, 期 45, 页码 13170-13184

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201502493

关键词

alkylation; asymmetric catalysis; carbanions; nitriles; synthetic methods

资金

  1. University of the Basque Country UPV/EHU [UFI 11/22]
  2. Basque Government [IT-628-13]
  3. Ministerio de Economia y Competitividad [CTQ2013-47925-C2]

向作者/读者索取更多资源

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, -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.

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