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Samarium diiodide induced asymmetric synthesis of γ-butyrolactone using chiral auxiliaries derived from isosorbide and isomannide
引用本文:徐明华,林国强,夏立钧. Samarium diiodide induced asymmetric synthesis of γ-butyrolactone using chiral auxiliaries derived from isosorbide and isomannide[J]. 中国化学, 1998, 16(6): 561-564. DOI: 10.1002/cjoc.19980160613
作者姓名:徐明华  林国强  夏立钧
作者单位:Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 200032,China,Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 200032,China,Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 200032,China
基金项目:Project (No. 297912045) supported by the National Natural Science Foundation of China
摘    要:The asymmetric reductive coupling reaction of various acrylates derived from D-isosorbide and D-isomannide with acetophenone mediated by samarium diiodide to give both enan-tiomers of the optically active γ-butyrolactone was described.The best enantiomeric excess of the products was 60%.

关 键 词:Asymmetry  γ-butyrolactone   isosorbide   isonrannide   samarium diiodide

Samarium diiodide induced asymmetric synthesis of γ-butyrolactone using chiral auxiliaries derived from isosorbide and isomannide
XU,Ming-Hua LIN,Guo-Qiang XIA,Li-Jun. Samarium diiodide induced asymmetric synthesis of γ-butyrolactone using chiral auxiliaries derived from isosorbide and isomannide[J]. Chinese Journal of Chemistry, 1998, 16(6): 561-564. DOI: 10.1002/cjoc.19980160613
Authors:XU  Ming-Hua LIN  Guo-Qiang XIA  Li-Jun
Affiliation:XU,Ming-Hua LIN,Guo-Qiang XIA,Li-JunShanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 200032,China
Abstract:The asymmetric reductive coupling reaction of various acrylates derived from D-isosorbide and D-isomannide with acetophenone mediated by samarium diiodide to give both enantiomers of the optically active γ-butyrolactone was described. The best enantiomeric excess of the products was 60%.
Keywords:Asymmetry  γ-butyrolactone  isosorbide  isomannide  samarium diiodide
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