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Efficient and Facile Synthesis of ( ± )-Salvirecognine
引用本文:PENG Xuan-Jia,SHE Xue-Gong,BIE Ping-Yan,PAN Xin-Fu.Efficient and Facile Synthesis of ( ± )-Salvirecognine[J].有机化学,2003,23(Z1):436-436.
作者姓名:PENG Xuan-Jia  SHE Xue-Gong  BIE Ping-Yan  PAN Xin-Fu
作者单位:PENG Xuan-Jia(Department of Chemishty, State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000)  SHE Xue-Gong(Department of Chemishty, State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000)  BIE Ping-Yan(Department of Chemishty, State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000)  PAN Xin-Fu(Department of Chemishty, State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000)
摘    要:Salvirecognine (7) is a diterpene isolated from Salvia recognita1] which has been the subject of continued and growing interest, due to the range of biological activities shown by many members of this family. 2] In order to study further relationships between the structure and biological activity of the diterpene compounds and as an extension of diterpenoid synthesis in our laboratory, 3,4] the first total synthesis of the title compound was achieved by an efficient and facile route (Scheme 1).


Efficient and Facile Synthesis of ( ± )-Salvirecognine
Peng Xuan-jia,SHE Xue-gong,BIE Ping-Yan,PAN Xin-Fu.Efficient and Facile Synthesis of ( ± )-Salvirecognine[J].Chinese Journal of Organic Chemistry,2003,23(Z1):436-436.
Authors:Peng Xuan-jia  SHE Xue-gong  BIE Ping-Yan  PAN Xin-Fu
Abstract:Salvirecognine (7) is a diterpene isolated from Salvia recognita1] which has been the subject of continued and growing interest, due to the range of biological activities shown by many members of this family. 2] In order to study further relationships between the structure and biological activity of the diterpene compounds and as an extension of diterpenoid synthesis in our laboratory, 3,4] the first total synthesis of the title compound was achieved by an efficient and facile route (Scheme 1).
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