| Literature DB >> 24944521 |
Allen Y Hong1, Brian M Stoltz1.
Abstract
All-carbon quaternary stereocenters have posed significant challenges in the synthesis of complex natural products. These important structural motifs have inspired the development of broadly applicable palladium-catalyzed asymmetric allylic alkylation reactions of unstabilized non-biased enolates for the synthesis of enantioenriched α-quaternary products. This microreview outlines key considerations in the application of palladium-catalyzed asymmetric allylic alkylation reactions and presents recent total syntheses of complex natural products that have employed these powerful transformations for the direct, catalytic, enantioselective construction of all-carbon quaternary stereocenters.Entities:
Keywords: All-carbon quaternary stereocenters; Allylation; Asymmetric catalysis; Natural products; Palladium; Total synthesis
Year: 2013 PMID: 24944521 PMCID: PMC4059687 DOI: 10.1002/ejoc.201201761
Source DB: PubMed Journal: European J Org Chem ISSN: 1099-0690