Copper-Catalyzed Regioselective Silaboration of Aryl Allenes
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초록

We report a copper-catalyzed silaboration of aryl-substituted terminal allenes with a silylborane reagent (PhMe2Si-Bpin) that furnishes silyl-substituted allylboronates with good regioand stereoselectivity under mild conditions. A range of aryl allenes bearing electron-donating or electron-withdrawing groups afforded the corresponding allylboronate products in good to excellent yields (up to 97%) with high regioand stereocontrol. This method expands copper-catalyzed silaboration of terminal allenes from alkyl-substituted to aryl-substituted substrates.

키워드

coppersilaborationaryl allenesregioselectivityallylboronatesACTIVATIONMECHANISM
제목
Copper-Catalyzed Regioselective Silaboration of Aryl Allenes
저자
Lee, SungheeYoon, Wan SeokYun, Jaesook
DOI
10.1055/a-2833-1649
발행일
2026-04-07
유형
Article; Early Access
저널명
Synthesis