Synlett 2014; 25(07): 905-910
DOI: 10.1055/s-0033-1340621
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© Georg Thieme Verlag Stuttgart · New York

Metal-Free-Catalyzed Intramolecular Carbocyanation of Activated Alkenes: New Entry To Access Functionalized Nitriles Containing Quaternary Carbon Centers

Authors

  • Zhe Zhuang

    Department of Organic Chemistry, College of Chemistry, Jilin University, 2699 Qianjin Street, Changchun 130012, P. R. of China   Fax: +86(431)85153812   eMail: wliao@jlu.edu.cn
  • Wei-Wei Liao*

    Department of Organic Chemistry, College of Chemistry, Jilin University, 2699 Qianjin Street, Changchun 130012, P. R. of China   Fax: +86(431)85153812   eMail: wliao@jlu.edu.cn
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Publikationsverlauf

Received: 17. November 2013

Accepted after revision: 12. Dezember 2013

Publikationsdatum:
05. Februar 2014 (online)


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Abstract

Intramolecular carbocyanation reaction of alkenes has emerged as a powerful tool for preparing functionalized nitriles. In contrast to transition-metal-catalyzed processes, we have recently developed a metal-free carbocyanation (alkenylcyanation and acylcyanation) approach to construct functionalized nitriles incorporating a quaternary carbon center. This article summarizes our recent exploratory studies in this field.