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Aldehydeallylation with allylboronates providing α-addition products†
Shū Kobayashi,Toshimitsu Endo,Uwe Schneider,Masaharu Ueno
Chemical Communications Pub Date : 01/18/2010 00:00:00 , DOI:10.1039/B924527H
Abstract

Zn(OH)2-catalyzed allylation reactions of allylboronates with aldehydes proceeded smoothly in aqueous media; when α-substituted allylboronates were employed, the α-addition products were obtained exclusively, and syn-adducts were formed selectively in most cases; the use of Zn(OH)2 with dmp (ligand) in aqueous media is the key to these reactions.

Graphical abstract: Aldehyde allylation with allylboronates providing α-addition products
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