| Literature DB >> 30748069 |
Takuya Kochi1, Kazuya Ichinose1, Masayuki Shigekane1, Taro Hamasaki1, Fumitoshi Kakiuchi1.
Abstract
Sequential formation of distant bonds in organic molecules was achieved for the palladium-catalyzed hydrosilylation/cyclization of various 1,n-dienes by chain walking of the metal catalyst. The reaction was applicable to various 1,n-dienes, including a 1,13-diene, to form a cyclopentane ring as well as a carbon-silicon bond at a remote site. The use of "nondissociative" chain walking provides a fascinating strategy in organic synthesis to functionalize distant parts of organic molecules, in a particular order, within a catalytic cycle by effectively moving the reactive center from a remote position.Entities:
Keywords: alkenes; cyclizations; hydrosilylation; isomerizations; palladium
Year: 2019 PMID: 30748069 DOI: 10.1002/anie.201814558
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336