4.8 Article

Silver-catalyzed remote Csp3-H functionalization of aliphatic alcohols

Journal

NATURE COMMUNICATIONS
Volume 9, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-018-05014-w

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Funding

  1. National Natural Science Foundation of China [21632001, 21772002]
  2. National Basic Research Program of China (973 Program) [2015CB856600]
  3. National Young Top-Notch Talent Support Program
  4. Peking University Health Science Center [BMU20160541]

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Aliphatic alcohols are common and bulk chemicals in organic synthesis. The site-selective functionalization of non-activated aliphatic alcohols is attractive but challenging. Herein, we report a silver-catalyzed d-selective Csp(3)-H bond functionalization of abundant and inexpensive aliphatic alcohols. Valuable oximonitrile substituted alcohols are easily obtained by using well-designed sulphonyl reagents under simple and mild conditions. This protocol realizes the challenging d-selective C-C bond formation of simple alkanols.

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