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Catalytic asymmetric aldehyde prenylation and application in the total synthesis of (−)-rosiridol and (−)-bifurcadiol†
Yu-Long Zhang,Zhen-Ni Zhao,Wang-Lai Li,Jing-Jie Li,Subarna Jyoti Kalita,Uwe Schneider,Yi-Yong Huang
Chemical Communications Pub Date : 07/20/2020 00:00:00 , DOI:10.1039/D0CC00367K
Abstract

Chiral phosphoric acid-catalyzed asymmetric aldehyde prenylation has been established using an α,α-dimethyl allyl boronic ester. The transformation provides expedient access to a wide array of aryl, heteroaryl, aryl-substituted alkenyl and primary and secondary aliphatic homoprenyl alcohols with excellent asymmetric induction. The utility of this asymmetric catalysis strategy has been demonstrated through a short and efficient total synthesis of the two natural products (−)-rosiridol and (−)-bifurcadiol.

Graphical abstract: Catalytic asymmetric aldehyde prenylation and application in the total synthesis of (−)-rosiridol and (−)-bifurcadiol
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