4.8 Article

Aminoazanium of DABCO: An Amination Reagent for Alkyl and Aryl Pinacol Boronates

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 59, 期 7, 页码 2745-2749

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201913388

关键词

amination; arenes; amines; boron; synthetic methods

资金

  1. National Natural Science Foundation of China [91745110, 21673261, 21603245, 21703265, 21872156, 21802150, 21773210, 21603190]
  2. Natural Science Foundation of Jiangsu Province [BK20190002, BK20181194, BK20180247]
  3. Young Elite Scientist Sponsorship Program by CAST [YESS20170217]
  4. Youth Innovation Promotion Association CAS [2018458]

向作者/读者索取更多资源

The aminoazanium of DABCO (H2N-DABCO) has been developed as a general and practical amination reagent for the direct amination of alkyl and aryl pinacol boronates. This compound is stable and practical for use as a reagent. Various primary, secondary. and tertiary alkyl-Bpin and aryl-Bpin substrates were aminated to give the corresponding amine derivatives. The amination is stereospecific. The anti-Markovnikov hydroamination of olefins was easily achieved by catalytic hydroboration with HBpin and in subsequent situ amination using H2N-DABCO. Moreover, the combination of 1,2-diboration of olefins, using B(2)pin(2), with this amination process achieved the unprecedented 1,2-diamination of olefins. The amination protocol was also successfully extended to aryl pinacol boronates.

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