中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Difluorination of Furonaphthoquinones

文献类型:期刊论文

作者Li, Jie1; Xue, Yu2; Fan, Zhoulong3,4,5; Ding, Chunyong3,5; Zhang, Ao1,3,4,5
刊名JOURNAL OF ORGANIC CHEMISTRY
出版日期2017-07-21
卷号82期号:14页码:7388-7393
ISSN号0022-3263
DOI10.1021/acs.joc.7b01064
文献子类Article
英文摘要An unprecedented difluorination reaction was developed based on the furonaphthoquinone skeleton of natural products tanshinones and their analogues. By using Selectfluor as the fluorinating source and H2O as the hydroxyl source, a wide range of unique polycyclic alpha,alpha-difluoro beta,beta-dihydroxyl para-quinone products were achieved with yields up to 90%. The mechanistic studies revealed that the reaction might undergo tandem multiple electrophilic and nucleophilic substitutions, as well as cleavages of C-O and C-C bonds. This approach not only provides a new method to synthesis of alpha,alpha-difluoro ketones, but also affords a series of unique chemotypes for biological activity screening.
WOS关键词PRODUCT TANSHINONE IIA ; DIFLUOROMETHYL KETONES ; MEDICINAL CHEMISTRY ; SALVIA-MILTIORRHIZA ; CARBONYL-COMPOUNDS ; ACID-CHLORIDES ; PLASMEPSIN II ; DERIVATIVES ; INHIBITORS ; FLUORINE
资助项目National Natural Science Foundation of China[81373277] ; National Natural Science Foundation of China[81402790] ; International Cooperative Program[GJHZ1622] ; Frontier Science of the Chinese Academy of Sciences[160621] ; Shanghai Commission of Science and Technology[16XD1404600] ; Shanghai Commission of Science and Technology[14431905300] ; Shanghai Commission of Science and Technology[14431900400]
WOS研究方向Chemistry
语种英语
WOS记录号WOS:000406355900031
出版者AMER CHEMICAL SOC
源URL[http://119.78.100.183/handle/2S10ELR8/272560]  
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Ding, Chunyong; Zhang, Ao
作者单位1.ShanghaiTech Univ, Shanghai 201210, Peoples R China;
2.China Pharmaceut Univ, Dept Med Chem, Nanjing 210009, Jiangsu, Peoples R China;
3.Chinese Acad Sci, Shanghai Inst Mat Med, CAS Key Lab Receptor Res, Shanghai 201203, Peoples R China;
4.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China;
5.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
推荐引用方式
GB/T 7714
Li, Jie,Xue, Yu,Fan, Zhoulong,et al. Difluorination of Furonaphthoquinones[J]. JOURNAL OF ORGANIC CHEMISTRY,2017,82(14):7388-7393.
APA Li, Jie,Xue, Yu,Fan, Zhoulong,Ding, Chunyong,&Zhang, Ao.(2017).Difluorination of Furonaphthoquinones.JOURNAL OF ORGANIC CHEMISTRY,82(14),7388-7393.
MLA Li, Jie,et al."Difluorination of Furonaphthoquinones".JOURNAL OF ORGANIC CHEMISTRY 82.14(2017):7388-7393.

入库方式: OAI收割

来源:上海药物研究所

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