| Literature DB >> 17878971 |
Thierry Ollevier1, Etienne Nadeau.
Abstract
In the presence of a catalytic amount of Bi(OTf)(3).4H(2)O, aldehydes together with amines react with silyl enolates to afford the corresponding Mannich-type adducts smoothly. A wide variety of silyl enolates derived from ketones, as well as esters and thioesters, react rapidly to afford the beta-amino ketones or the beta-amino esters in high yields (up to 94%).Entities:
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Year: 2007 PMID: 17878971 DOI: 10.1039/b710794c
Source DB: PubMed Journal: Org Biomol Chem ISSN: 1477-0520 Impact factor: 3.876