| Literature DB >> 12917003 |
Yutaka Suto1, Naoya Kumagai, Shigeki Matsunaga, Motomu Kanai, Masakatsu Shibasaki.
Abstract
[reaction: see text] A copper fluoride-catalyzed cyanomethylation that can be applied to a wide range of ketones and aldehydes was developed using TMSCH(2)CN as a nucleophile. The reaction was extended to a conceptually more advanced copper alkoxide-catalyzed direct addition of alkylnitriles to aldehydes, which can act as a surrogate direct catalytic aldol reaction of esters. These reactions can be applied to the first catalytic enantioselective cyanomethylation of ketones and direct catalytic enantioselective cyanomethylation of aldehydes.Entities:
Year: 2003 PMID: 12917003 DOI: 10.1021/ol035206u
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005