Journal
NATURE COMMUNICATIONS
Volume 9, Issue -, Pages -Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-018-05014-w
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Funding
- National Natural Science Foundation of China [21632001, 21772002]
- National Basic Research Program of China (973 Program) [2015CB856600]
- National Young Top-Notch Talent Support Program
- 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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