中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Enantioselective Total Synthesis of (-)-HosieineA

文献类型:期刊论文

作者Ou YJ(欧阳杰); Yan R(严睿); Mi XW(米贤伟); Hong R(洪然)
刊名Angew. Chem.-Int. Edit.
出版日期2015
卷号54期号:37页码:10940-10943
其他题名(?)-Hosieine A的对映选择性全合成
通讯作者洪然
英文摘要The first total synthesis of (-)-hosieineA was accomplished and features an unprecedented nitroso-ene cyclization to construct the 2-azabicyclo[3.2.1]octane ring system. Phosphine-enabled stereoselective bromohydrination provided interesting mechanistic insights into the anti-Markovnikov process. Also noteworthy is the retention of stereochemistry at C9 in the facile radical debromination initiated by Et3B/air.
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/10.1002/anie.201505251
语种英语
WOS记录号WOS:000360628500044
源URL[http://ir.sioc.ac.cn/handle/331003/39804]  
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
作者单位中科院上海有机化学研究所, 天然产物有机合成化学重点实验室
推荐引用方式
GB/T 7714
Ou YJ,Yan R,Mi XW,et al. Enantioselective Total Synthesis of (-)-HosieineA[J]. Angew. Chem.-Int. Edit.,2015,54(37):10940-10943.
APA 欧阳杰,严睿,米贤伟,&洪然.(2015).Enantioselective Total Synthesis of (-)-HosieineA.Angew. Chem.-Int. Edit.,54(37),10940-10943.
MLA 欧阳杰,et al."Enantioselective Total Synthesis of (-)-HosieineA".Angew. Chem.-Int. Edit. 54.37(2015):10940-10943.

入库方式: OAI收割

来源:上海有机化学研究所

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