Stereoselective synthesis of (+/-)-tacamonine
He ZL(何子乐) ; Lin QX(林其先)
刊名Tetrahedron
2008
卷号64期号:45页码:10401-10405
ISSN号0040-4020
其他题名Stereoselective synthesis of (+/-)tacamonine
通讯作者何子乐
英文摘要We report a stereocontrolled approach to the pentacyclic indole alkaloid tacamonine by modifying an earlier route using norbornadiene to supply the nontryptamine portion. By maintaining a bridged system the reduction step of the Bischler-Napieralski reaction proceeded to deliver a bridged diol in which three methine hydrogen atoms are in an all-cis configuration. All 19 skeletal carbon atoms are fully incorporated, therefore, the only remaining steps involved cleavage of the vic-diol subunit in the seven-membered ring and further oxidation and reduction of the resulting lactam alclehyde. (C) 2008 Elsevier Ltd. All rights reserved.
学科主题天然产物有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1016/j.tet.2008.08.049
语种英语
WOS记录号WOS:000260290900013
公开日期2013-08-14
内容类型期刊论文
源URL[http://202.127.28.38/handle/331003/27703]  
专题上海有机化学研究所_上海有机化学研究所
推荐引用方式
GB/T 7714
He ZL,Lin QX. Stereoselective synthesis of (+/-)-tacamonine[J]. Tetrahedron,2008,64(45):10401-10405.
APA 何子乐,&林其先.(2008).Stereoselective synthesis of (+/-)-tacamonine.Tetrahedron,64(45),10401-10405.
MLA 何子乐,et al."Stereoselective synthesis of (+/-)-tacamonine".Tetrahedron 64.45(2008):10401-10405.
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