| Literature DB >> 24760480 |
Christoph Schneider1, Falko Abels.
Abstract
Recent progress in the field of catalytic, enantioselective vinylogous Michael reactions of latent dienolates is described which furnish optically highly enriched chiral 1,7-dioxo compounds of great utility in one synthetic operation. Emphasis is given to new catalysis modes which realise this challenging transformation with high regio- as well as enantioselectivity.Entities:
Year: 2014 PMID: 24760480 DOI: 10.1039/c4ob00332b
Source DB: PubMed Journal: Org Biomol Chem ISSN: 1477-0520 Impact factor: 3.876