| Literature DB >> 30431281 |
Aiyou Xia1, Xin Xie1, Haoyi Chen1, Jidong Zhao1, Chunli Zhang1, Yuanhong Liu1.
Abstract
A nickel-catalyzed cyanation of unactivated secondary alkyl chlorides or bromides using less toxic Zn(CN)2 as the cyanide source has been developed. The reaction features the use of air-stable and inexpensive NiCl2·6H2O or Ni(acac)2 as the precatalysts and offers an efficient synthesis of a broad range of alkyl nitriles. Cyanation of primary alkyl chlorides or bromides was also achieved by reaction with Zn(CN)2 in the presence of n-Bu4NCl without the need of nickel catalyst.Entities:
Year: 2018 PMID: 30431281 DOI: 10.1021/acs.orglett.8b03539
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005