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.