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Regioselective etherification of 1,2-O-isopropylidene-4,6-di-O-benzyl myo-inositol
作者姓名:YUAN  Cheng-Ye ZHAI  Hai-Xiao LI  Shu-SenShanghai Institute of Organic Chemistry  Chinese Academy of Sciences  Shanghai S  China
作者单位:YUAN,Cheng-Ye ZHAI,Hai-Xiao LI,Shu-SenShanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 20003S,China
基金项目:Project supported by the National Natural Science Foundation of China.
摘    要:During the etherification of 1,2-O-isopropylidene-4,6-di-O-benzyl myo-inositol, the specific regioselectivity on 3- or 5-hydroxyl group was showed to be determined by the nature of the O-alkylating agents used. As demonstrated by MM and MNDO calculation, the regioselectivity of the reaction mentioned can be rationalized by steric and/or electronic effect.


Regioselective etherification of 1,2-O-isopropylidene-4,6-di-O-benzyl myo-inositol
YUAN,Cheng-Ye ZHAI,Hai-Xiao LI,Shu-SenShanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai S,China.Regioselective etherification of 1,2-O-isopropylidene-4,6-di-O-benzyl myo-inositol[J].Chinese Journal of Chemistry,1996(3).
Authors:YUAN  Cheng-Ye ZHAI  Hai-Xiao LI  Shu-Sen
Institution:YUAN,Cheng-Ye ZHAI,Hai-Xiao LI,Shu-SenShanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 20003S,China
Abstract:During the etherification of 1,2-O-isopropylidene-4,6-di-O-benzyl myo-inositol, the specific regioselectivity on 3- or 5-hydroxyl group was showed to be determined by the nature of the O-alkylating agents used. As demonstrated by MM and MNDO calculation, the regioselectivity of the reaction mentioned can be rationalized by steric and/or electronic effect.
Keywords:Regioselective  etherification  myo-inositol  MM and MNDO calculation
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