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Efficient Synthesis of 2—Ethyl—A—ring Analogues of 19—Nor—1α,25—dihydroxy Vitamin D3
作者姓名:WangQiu-an  ZHAOYu-rui
作者单位:[1]ColllegeofchemistryandChemicalEngineering,HunanUniversity,Changsha410082,P.R.China [2]DepartmentofOrganicChemistry,UniversityofGent,Krijgslaan281S4,B-9000Gent,Belgium
摘    要:The novel 19-nor-1α,25-dihydroxy vitamin D3 analogues possessing an ethyl at the 2-position(4 and 5).were synthesized by coupling 25-hydroxy Windaus-Grundmann ketone derivative 20 with A-ring synthons(15 and 19)respectively.The enantioselective synthesis of substituted bicyclic3,1,0]hexanes structure A-ring synthons,started from all-cis-3,5-dihydroxy-4-ethyl-1-(methoxycarbonyl)cyclohexane via lipase-catalyzd asymmetrization,was demonstratcd.

关 键 词:维生素D3  乙烷基环状物  类似物  合成

Efficient Synthesis of 2-Ethyl-A-ring Analogues of 19-Nor-1α,25-dihydroxy Vitamin D3
WangQiu-an ZHAOYu-rui.Efficient Synthesis of 2-Ethyl-A-ring Analogues of 19-Nor-1α,25-dihydroxy Vitamin D3[J].Chemical Research in Chinese University,2003,19(2):165-173.
Authors:WANG Qiuan  ZHAO Yu-rui
Abstract:The novel 19-nor-lα,25-dihydroxy vitamin D3 analogues possessing an ethyl at the 2-position(4 and 5), were synthesized by coupling 25-hydroxy Windaus-Grundmann ketone derivative 20 with A-ring synthons(15 and 19) respectively. The enantioselective synthesis of substituted bicyclic3,1,0] hexanes structure A-ring synthons, started from all-cis-3,5-dihydroxy-4-ethyl-1-(methoxycarbonyl)cyclohexane via lipase-catalyzd asymmetrization, was demonstrated.
Keywords:25-dihydroxy vitamin D3  Synthesis  Lipase-catalyzed  Asymmetrization
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