Synthetic Study on Tetrapetalones: Stereoselective Cyclization of N-Acyliminium Ion To Construct Substituted 1-Benzazepines
Li C(李程) ; Li XY(李新宇) ; Hong R(洪然)
刊名Org. Lett.
2009
卷号11期号:18页码:4036-4039
ISSN号1523-7060
其他题名Synthetic Study on Tetrapetalones: Stereoselective Cyclization of N-Acyliminium Ion To Construct Substituted 1-Benzazepines
通讯作者洪然
英文摘要The synthesis of the tetracyclic core of complex antibiotic tetrapetalones has been achieved in three steps starting from the simple intermediate gamma-hydroxy amide, which can be accessed through a high-yielding six-step sequence. The successful synthesis relies on a novel strategy based on the N-acyliminium ion cyclization.
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/10.1021/ol901349b
语种英语
WOS记录号WOS:000269670700003
公开日期2013-08-29
内容类型期刊论文
源URL[http://202.127.28.38/handle/331003/28581]  
专题上海有机化学研究所_中科院天然产物有机化学重点实验室
推荐引用方式
GB/T 7714
Li C,Li XY,Hong R. Synthetic Study on Tetrapetalones: Stereoselective Cyclization of N-Acyliminium Ion To Construct Substituted 1-Benzazepines[J]. Org. Lett.,2009,11(18):4036-4039.
APA 李程,李新宇,&洪然.(2009).Synthetic Study on Tetrapetalones: Stereoselective Cyclization of N-Acyliminium Ion To Construct Substituted 1-Benzazepines.Org. Lett.,11(18),4036-4039.
MLA 李程,et al."Synthetic Study on Tetrapetalones: Stereoselective Cyclization of N-Acyliminium Ion To Construct Substituted 1-Benzazepines".Org. Lett. 11.18(2009):4036-4039.
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