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Remarkable Stereoelectronic Effect of the Methylenedioxy Phenyl System in the Total Synthesis of Cephalotaxine
引用本文:HuaYANG YongQiangWANG WeiDongZ.LI. Remarkable Stereoelectronic Effect of the Methylenedioxy Phenyl System in the Total Synthesis of Cephalotaxine[J]. 中国化学快报, 2005, 16(3): 311-314
作者姓名:HuaYANG YongQiangWANG WeiDongZ.LI
作者单位:StateKeyLaboratoryofAppliedOrganicChemistry,LanzhouUniversity,Lanzhou730000
摘    要:Methylenedioxyphenyl unit displays a significant stereoelectronic effect in some key transformations in the total synthesis of cephalotaxine. The ring-strain of methylenedioxy ring may account for some important facile ring-skeleton rearrangements.

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Remarkable Stereoelectronic Effect of the Methylenedioxy Phenyl System in the Total Synthesis of Cephalotaxine
Hua YANG Yong Qiang WANG,Wei Dong Z. LI State Key Laboratory of Applied Organic Chemistry,Lanzhou University,Lanzhou. Remarkable Stereoelectronic Effect of the Methylenedioxy Phenyl System in the Total Synthesis of Cephalotaxine[J]. Chinese Chemical Letters, 2005, 16(3): 311-314
Authors:Hua YANG Yong Qiang WANG  Wei Dong Z. LI State Key Laboratory of Applied Organic Chemistry  Lanzhou University  Lanzhou
Affiliation:Hua YANG Yong Qiang WANG,Wei Dong Z. LI* State Key Laboratory of Applied Organic Chemistry,Lanzhou University,Lanzhou 730000
Abstract:Methylenedioxyphenyl unit displays a significant stereoelectronic effect in some key transformations in the total synthesis of cephalotaxine. The ring-strain of methylenedioxy ring may account for some important facile ring-skeleton rearrangements.
Keywords:Stereoelectronic effect   reductive rearrangement   cephalotaxine   total synthesis.
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