| Literature DB >> 21718038 |
Matthew G Beaver1, Timothy F Jamison.
Abstract
A Ni-catalyzed reductive coupling of alkynes and epoxides using Ni(II) salts and simple alcohol reducing agents is described. Whereas previously reported conditions relied on Ni(cod)(2) and Et(3)B, this system has several advantages including the use of air-stable and inexpensive Ni(II) precatalysts (e.g., NiBr(2)·3H(2)O) as the source of Ni(0) and simple alcohols (e.g., 2-propanol) as the reducing agent. Deuterium-labeling experiments are consistent with oxidative addition of an epoxide C-O bond that occurs with inversion of configuration.Entities:
Mesh:
Substances:
Year: 2011 PMID: 21718038 PMCID: PMC3148188 DOI: 10.1021/ol201702a
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005