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Site-selective deuteration at the α-position of enals by an amine and bis(phenylsulfonyl)methane co-catalyzed H/D exchange reaction†
Shilei Zhang,Fan Luo,Jiarui Wang,Xinyu Zhang,Xuejun Liu,Xiaodong Chen,Xiaobei Chen
Chemical Communications Pub Date : 09/15/2022 00:00:00 , DOI:10.1039/D2CC04959G
Abstract

An amine and bis(phenylsulfonyl)methane co-catalyzed hydrogen–deuterium exchange (HDE) method via a Michael-retro-Michael pathway for site-selective introduction of deuterium at the α-position of enals using D2O as a deuterium source has been achieved. The mild, operationally simple protocol allows for high yielding and high level deuterium incorporation (up to 99%) for structurally diverse aromatic-derived enals and dienals.

Graphical abstract: Site-selective deuteration at the α-position of enals by an amine and bis(phenylsulfonyl)methane co-catalyzed H/D exchange reaction
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