中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
An Organic Molecule Modulated Chemoselective Cyclization of Alkynyl Nitriles Tethered to 2-Alkyl Substituted Chromones with Multireactive Sites

文献类型:期刊论文

作者Huang, Liping; Liu, Yang; Xie, Fuchun; Hu, Youhong
刊名ORGANIC LETTERS
出版日期2012-12-21
卷号14期号:24页码:6122-6125
ISSN号1523-7060
DOI10.1021/ol302964x
文献子类Article
英文摘要A small organic molecule phenylacetonitrile promoted chemoselective cyclization of (chromen-3-yl)alkynylnitriles to generate a novel tetracyclic or tricyclic chromone scaffold has been discovered. Importantly, the phenylacetonitrile serves as an anion transfer reagent changing the normal reaction of the substrate.
WOS关键词PALLADIUM-CATALYZED CARBOANNULATION ; PROPARGYLIC CARBONATES ; INDENE DERIVATIVES ; 5-ENDO-DIG CARBOCYCLIZATION ; ELECTROPHILIC CYCLIZATION ; 1,3-DICARBONYL COMPOUNDS ; EFFICIENT APPROACH ; BETA-KETOESTERS ; TANDEM REACTION ; NUCLEOPHILES
资助项目National Natural Science Foundation of China[21172232] ; Ministry of Science and Technology of China[2009CB940903]
WOS研究方向Chemistry
语种英语
WOS记录号WOS:000312564500002
出版者AMER CHEMICAL SOC
源URL[http://119.78.100.183/handle/2S10ELR8/277840]  
专题药物化学研究室
中科院受体结构与功能重点实验室
新药研究国家重点实验室
通讯作者Hu, Youhong
作者单位Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Beijing 100864, Peoples R China
推荐引用方式
GB/T 7714
Huang, Liping,Liu, Yang,Xie, Fuchun,et al. An Organic Molecule Modulated Chemoselective Cyclization of Alkynyl Nitriles Tethered to 2-Alkyl Substituted Chromones with Multireactive Sites[J]. ORGANIC LETTERS,2012,14(24):6122-6125.
APA Huang, Liping,Liu, Yang,Xie, Fuchun,&Hu, Youhong.(2012).An Organic Molecule Modulated Chemoselective Cyclization of Alkynyl Nitriles Tethered to 2-Alkyl Substituted Chromones with Multireactive Sites.ORGANIC LETTERS,14(24),6122-6125.
MLA Huang, Liping,et al."An Organic Molecule Modulated Chemoselective Cyclization of Alkynyl Nitriles Tethered to 2-Alkyl Substituted Chromones with Multireactive Sites".ORGANIC LETTERS 14.24(2012):6122-6125.

入库方式: OAI收割

来源:上海药物研究所

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