School of Chemistry and Chemical
Engineering, South China University of Technology, Guangzhou 510641, China
Engineering, South China University of Technology, Guangzhou 510641, China
Org. Lett., Article ASAP
DOI: 10.1021/acs.orglett.6b01472
Publication Date (Web): June 16, 2016
Copyright © 2016 American Chemical Society
*E-mail: blyin@scut.edu.cn.
Abstract
A
protocol for the 2,5-oxyarylation of furan rings via Pd-catalyzed
aerobic oxidative coupling of boronic acids with α-hydroxyalkylfurans is
reported. This protocol provides rapid, green access to diverse
biologically interesting and synthetically useful unsaturated
spiroacetals from sustainable furan derivatives.
protocol for the 2,5-oxyarylation of furan rings via Pd-catalyzed
aerobic oxidative coupling of boronic acids with α-hydroxyalkylfurans is
reported. This protocol provides rapid, green access to diverse
biologically interesting and synthetically useful unsaturated
spiroacetals from sustainable furan derivatives.
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