| Literature DB >> 29202243 |
Julie L Hofstra1, Alan H Cherney1, Ciara M Ordner1, Sarah E Reisman1.
Abstract
An asymmetric Ni-catalyzed reductive cross-coupling has been developed to prepare enantioenriched allylic silanes. This enantioselective reductive alkenylation proceeds under mild conditions and exhibits good functional group tolerance. The chiral allylic silanes prepared here undergo a variety of stereospecific transformations, including intramolecular Hosomi-Sakurai reactions, to set vicinal stereogenic centers with excellent transfer of chirality.Entities:
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Year: 2017 PMID: 29202243 PMCID: PMC5851001 DOI: 10.1021/jacs.7b11707
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419