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Synthesis of Chlorin—enediyne Dyads by Palladium—catalyzed Coupling Reaction
引用本文:王进军 韩光范 殷军港 邬旭然 赵岩 宫宝安 沈荣基. Synthesis of Chlorin—enediyne Dyads by Palladium—catalyzed Coupling Reaction[J]. 中国化学, 2003, 21(6): 674-679. DOI: 10.1002/cjoc.20030210619
作者姓名:王进军 韩光范 殷军港 邬旭然 赵岩 宫宝安 沈荣基
作者单位:[1]DepartmentofAppliedChemistry,YantainUniversity,Yantai,Shandong264005,China [2]SchoolofMaterialScienceandEngineering,EastChinaShipbuildingInstitute,Zhenjiang,Jiangsu212003,China [3]BioorganicScienceDivision,KoreaResearchInstituteofTechnology,100Jang-Dong,Yusong-Gu,Taejon305-600,Korea
基金项目:ProjectsupportedbytheMinistryoftheScienceandTechnologyofChinaasacooperativeProjectbetweenChinaandKorea ( 2 0 0 2 )
摘    要:Methyl 9-ethylenedioxpyropheophorbide-d was prepared from methyl pyropheophorbide-a by protection of cyclic ketone with ethylene glycol,and oxidation with OsO4 in vinyl group at 2-position.The terminal alkyne was introduced into chlorin chromophore by Grignard reaction,and the enediyne moiety was constructed by a palladium-catalyzed coupling reaction with (Z)-chloroenynes.

关 键 词:合成 氯-烯二炔 抗癌药物 光疗法

Synthesis of Chlorin-enediyne Dyads by Palladium-catalyzed Coupling Reaction
Wang Jin‐Jun,Yin Jun‐Gang,Wu Xu‐Ran,Zhao Yan,Gong Bao‐An,Han Guang‐Fan,Shim Young Key. Synthesis of Chlorin-enediyne Dyads by Palladium-catalyzed Coupling Reaction[J]. Chinese Journal of Chemistry, 2003, 21(6): 674-679. DOI: 10.1002/cjoc.20030210619
Authors:Wang Jin‐Jun  Yin Jun‐Gang  Wu Xu‐Ran  Zhao Yan  Gong Bao‐An  Han Guang‐Fan  Shim Young Key
Abstract:Methyl 9 ethylenedioxpyropheophorbide d was prepared from methyl pyropheophorbide a by protection of cyclic ketone with ethylene glycol, and oxidation with OsO 4 in vinyl group at 2 position. The terminal alkyne was introduced into chlorin chromophore by Grignard reaction, and the enediyne moiety was constructed by a palladium catalyzed coupling reaction with (Z) chloroenynes.
Keywords:enediyne   chlorin   chlorin enediyne dyads   photodynamic therapy   anticancer agent  
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