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First Total Synthesis of 4,5-Sccoeudesmane-type and Iphionane-type Compounds-Synthesis of 4,5-Dioxo-seco-γ-eudesmol and 5β,11-Dihydroxyiphionan-4-one

First Total Synthesis of 4,5-Sccoeudesmane-type and Iphionane-type Compounds-Synthesis of 4,5-Dioxo-seco-γ-eudesmol and 5β,11-Dihydroxyiphionan-4-one

作     者:Zhao Ming XIONG Gang ZHOU Xiao Lei GAO Yong Gang CHEN Yu lin LI (National Laboratory of Applied Organic Chemistry and Institute of organic Chemistry, Lanzhou University, Lanzhou 730000) 

作者机构:Natl. Lab. of Appl. Organ. Chemistry Institute of Organic Chemistry Lanzhou University Lanzhou 730000 China 

出 版 物:《Chinese Chemical Letters》 (中国化学快报(英文版))

年 卷 期:2000年第11卷第2期

页      面:113-114页

核心收录:

学科分类:081704[工学-应用化学] 07[理学] 08[工学] 0817[工学-化学工程与技术] 070303[理学-有机化学] 0703[理学-化学] 

基  金:the National Natural Science Foundation of China(29732060) The National Laboratory of Elemento-Organic Chemistry at Nankai University 

主  题:type First Total Synthesis of 4,5-Sccoeudesmane-type and Iphionane-type Compounds-Synthesis of 4,5-Dioxo-seco eudesmol and 5 Dihydroxyiphionan-4-one 

摘      要:4, 5-Secoeudesmane-type and iphionane-type compounds are sesquiterpenes with new carbon skeletons found in natrual sources in recent years.1-6 The co-occurence of 4, 5-secoeudesmanes, iphionanes and eudesmanes as natrual products suggests that 4, 5-secoeudesmanes, iphionanes most likely are generated biogenetically from eudesmanes, and iphionanes are formed biogenetically by aldol reaction of 4, 5-dioxosecoeudesmanes1,4,6,7. The study on the synthesis of this two kind of new sesquiterpenes has not been reported in the literature.

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