| Literature DB >> 31702842 |
Kento Ishida1, Hokuto Yamazaki1, Chihiro Hagiwara1, Manabu Abe2, Hiroyuki Kusama1.
Abstract
Acylsilanes have been known to undergo isomerization to siloxycarbenes under photoirradiation and the thus generated carbenes can be utilized for various synthetic reactions. But this carbene formation is not necessarily efficient with some alkanoylsilanes because Norrish-type fragmentations compete, which limit the synthetic utility of alkanoylsilanes as carbene precursors. In this study, generation of siloxycarbenes from alkanoylsilanes by visible-light-induced energy transfer was examined by using an Ir complex, [Ir{dF(CF3 )ppy}2 (dtbpy)]PF6 , and was successfully applied to the C-C coupling reactions with boronic esters or aldehydes. This methodology efficiently suppressed undesired Norrish-type reactions and broadened synthetic utility of alkanoylsilanes.Entities:
Keywords: acylsilanes; energy transfer; photochemistry; siloxycarbenes; triplet sensitizer
Year: 2020 PMID: 31702842 DOI: 10.1002/chem.201904635
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236