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Asymmetric Phase-Transfer-Catalyzed 1,6-Conjugate Addition of Thiols to in situ Generated para-Quinone Methides
ZHOU Lei,FAN Yajing,LI Shen * #
Department of Chemistry, School of Science, Tianjin University, Tianjin 300354
*Correspondence author
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Funding: the Specialized Research Fund for the Doctoral Program of Higher Education of China (No.No. 20130032120071)
Opened online:10 May 2017
Accepted by: none
Citation: ZHOU Lei,FAN Yajing,LI Shen.Asymmetric Phase-Transfer-Catalyzed 1,6-Conjugate Addition of Thiols to in situ Generated para-Quinone Methides[OL]. [10 May 2017] http://en.paper.edu.cn/en_releasepaper/content/4732205
 
 
A catalytic asymmetric 1,6-conjugate addition of thiols to in situ generated para-quinone methides has been developed, affording a range of optically active benzyl thioethers in excellent yields and enantioselectivities. The use of para-hydroxybenzyl sulfones as precursors for the formation of transient p-QM intermediates allows to overcome the limitations in substrate scope.
Keywords:Asymmetric catalysis; Phase-transfer catalysis; 1,6-Conjugate addition; para-quinone methide
 
 
 

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