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学科主题: 药学
题名:
Formal synthesis of semiaquilegin A
作者: Li, Jing1; Jiang, Yong1; Li, Qingjiang1; Xiao, Qiang2; Jia, Yanxing1; Tu, Pengfei1
关键词: Semiaquilegin A ; Oridonin ; Barton deoxygenation ; Formal synthesis
刊名: TETRAHEDRON LETTERS
发表日期: 2010-02-17
DOI: 10.1016/j.tetlet.2009.12.118
卷: 51, 期:7, 页:1121-1123
收录类别: SCI ; IC ; CCR
文章类型: Article
WOS标题词: Science & Technology
类目[WOS]: Chemistry, Organic
研究领域[WOS]: Chemistry
关键词[WOS]: ACID RELATED-COMPOUNDS ; SECONDARY ALCOHOLS ; EFFICIENT DEOXYGENATION ; GENERAL PROCEDURE ; NATURAL-PRODUCTS ; CYANOSAFRACIN B ; CONVERSION ; 2&prime ; -DEOXYNUCLEOSIDES ; RIBONUCLEOSIDES
英文摘要:

A formal synthesis of semiaquilegin A is achieved starting from readily available oridonin in 19 linear steps. The absolute configuration of the natural product has been established. A variety of useful analogues were prepared through this synthetic route. (C) 2009 Elsevier Ltd. All rights reserved.

语种: 英语
所属项目编号: 30600778
项目资助者: Peking University and National Natural Science Foundation of China
WOS记录号: WOS:000274477500031
Citation statistics:
内容类型: 期刊论文
URI标识: http://ir.bjmu.edu.cn/handle/400002259/58512
Appears in Collections:北京大学药学院_期刊论文

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作者单位: 1.Peking Univ, State Key Lab Nat & Biomimet Drugs, Sch Pharmaceut Sci, Beijing 100191, Peoples R China
2.Jiangxi Sci & Technol Normal Univ, Inst Organ Chem, Nanchang 330013, Peoples R China

Recommended Citation:
Li, Jing,Jiang, Yong,Li, Qingjiang,et al. Formal synthesis of semiaquilegin A[J]. TETRAHEDRON LETTERS,2010,51(7):1121-1123.
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