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(Salen)Ti(IV)-Catalyzed Asymmetric Ring-opening of Monosubstituted Epoxides with Dithiophosphorus Acid
Zhou Zhenghong * #,Wang Quanyong #,Liu Bing #,Guofeng Zhao,Qilin Zhou,Chuchi Tang
Nankai University
*Correspondence author
#Submitted by
Subject:
Funding: 教育部博士点基金(No.20020055002)
Opened online:24 November 2005
Accepted by: none
Citation: Zhou Zhenghong,Wang Quanyong,Liu Bing .(Salen)Ti(IV)-Catalyzed Asymmetric Ring-opening of Monosubstituted Epoxides with Dithiophosphorus Acid[OL]. [24 November 2005] http://en.paper.edu.cn/en_releasepaper/content/3769
 
 
The asymmetric ring-opening of monosubstituted epoxides with dithiophosphorus acids catalyzed by a (salen)Ti(IV) complex formed in situ from the reaction of Ti(OPr-i)4 and the chiral salen ligand derived from (1R,2R)-(+)-diaminocyclohexane and (R)-2,2’-diamino-1,1’- binaphthalene was realized. The resulting products were obtained with moderate enantioselectivity (up to 59% ee). High regioselectivity was observed for the alkyl substituted epoxides, whereas poor regioselectivity was obtained for the aryl substituted epoxides.
Keywords:(Salen)Ti(IV) complex, asymmetric ring-opening, monosubstituted epoxides, regioselectivity, enantioselectivity.
 
 
 

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