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题名: The enantioselective total synthesis of alkaloid (-)-galipeine
作者: Yang, PY;  Zhou, YG
刊名: TETRAHEDRON-ASYMMETRY
发表日期: 2004-04-05
DOI: 10.1016/j.tetasy.2004.02.012
卷: 15, 期:7, 页:1145-1149
收录类别: SCI ;  IC ;  CCR
文章类型: Article
WOS标题词: Science & Technology ;  Physical Sciences
类目[WOS]: Chemistry, Inorganic & Nuclear ;  Chemistry, Organic ;  Chemistry, Physical
研究领域[WOS]: Chemistry
英文摘要: The first total synthesis of (-)-galipeine was accomplished in seven steps with 54% overall yield from isovanillin based on Ir-catalyzed asymmetric hydrogenation of a quinoline derivative as a key step, with its absolute stereochemistry being established. (C) 2004 Elsevier Ltd. All rights reserved.
关键词[WOS]: GALIPEA-OFFICINALIS ;  HETEROAROMATIC-COMPOUNDS ;  HYDROGENATION ;  TETRAHYDROQUINOLINES
语种: 英语
WOS记录号: WOS:000220750800014
Citation statistics: 
内容类型: 期刊论文
URI标识: http://cas-ir.dicp.ac.cn/handle/321008/139537
Appears in Collections:中国科学院大连化学物理研究所_期刊论文

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作者单位: 1.Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China

Recommended Citation:
Yang, PY,Zhou, YG. The enantioselective total synthesis of alkaloid (-)-galipeine[J]. TETRAHEDRON-ASYMMETRY,2004,15(7):1145-1149.
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