4.4 Article

Direct oxidative cyanation of tertiary amines promoted by in situ generated hypervalent iodine(III)-CN intermediate

期刊

TETRAHEDRON LETTERS
卷 56, 期 41, 页码 5628-5631

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2015.08.058

关键词

alpha-Aminonitriles; Cyanation; N,N-Dialkylanilines; Hypervalent iodine; TMSCN

资金

  1. National Natural Science Foundation of China [21372265]
  2. Natural Science Foundation Project of CQ CSTC [cstc2013jcyjA0217]
  3. Fundamental Research Funds for the Central Universities [CQDXWL-2013-Z012, CDJZR14225502]
  4. Chongqing University Postgraduates' Innovation Project

向作者/读者索取更多资源

An environmentally benign and metal-free cyanation method of tertiary amines oxidated by hypervalent iodine(III) intermediate generated in situ from PIFA (or DIB) and TMSCN has been developed. A variety of substituent groups on amines are tolerated to the oxidation of alpha-C-H bond to form C-C bond in the absence of metal catalysts with yields of up to 74%. (C) 2015 Elsevier Ltd. All rights reserved.

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