학술논문

Engaging yne-allenones in tunable catalytic silane-mediated conjugate transfer reductions.
Document Type
Article
Source
Chemical Communications. 6/4/2021, Vol. 57 Issue 44, p5394-5397. 4p.
Subject
Language
ISSN
1359-7345
Abstract
New tunable catalytic [2+2] cycloaddition/silane-mediated conjugate transfer reductions of yne-allenones have been developed, by which substituent-diverse cyclobutarenes with generally good yields were selectively synthesized by adjusting Fe – H and Cu – H catalytic systems. Use of the Fe – H system triggers 1,6-conjugate reduction to dihydrocyclobuta[a]naphthalen-4-ols whereas the Cu–H complex enables 1,4-conjugate reduction to cyclobuta[a]naphthalen-4(2H)-ones. [ABSTRACT FROM AUTHOR]