Journal
CHEMICAL COMMUNICATIONS
Volume 46, Issue 8, Pages 1260-1262Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b924527h
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- Japan Society for the Promotion of Science (JSPS)
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Zn(OH)(2)-catalyzed allylation reactions of allylboronates with aldehydes proceeded smoothly in aqueous media; when alpha-substituted allylboronates were employed, the a-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.
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