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Synthesis of 3,4-Dihalogenated Furan-2-(5H)-ones by Electrophilic Cyclization of 4-Hydroxy-2-alkynoates
Department固体润滑国家重点实验室
Zhu HT(祝海涛)1; Wang, Li-Jing1; Ji KG(纪克攻)1; Liu XY(刘雪原)1; Liang YM(梁永民)1,2; Liang YM(梁永民)
2012
Source PublicationChemistry - An Asian Journal
ISSN1861-4728
Volume7Issue:8Pages:1862-1866
AbstractFunctionalized 3,4-dihalogenated furan-2(5 H)-ones can be readily prepared in moderate to good yields by treating 4-hydroxy-4-arylbut-2-ynoate derivatives with ICl, IBr, and I2. Both halogen atoms of the electrophile are incorporated in the product. The resulting halides can further afford polycyclic aromatic compounds using known palladium-catalyzed coupling reactions.
KeywordAllenes Electrophilic Cyclization Furan-2(5h)-one Palladium Propargylic Alcohol
Subject Area材料科学与物理化学
DOI10.1002/asia.201200137
Funding Organizationthe National Science Foundation (NSF-21072080);the National Basic Research Program of China (973 Program) 2010CB8-33203;the "111" Project
Indexed BySCI
If4.572
Language英语
compositor第二作者单位
Citation statistics
Cited Times:13[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/19428
Collection固体润滑国家重点实验室(LSL)
Corresponding AuthorLiang YM(梁永民)
Affiliation1.Lanzhou Univ, Dept Chem, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China
2.Chinese Acad Sci, Lanzhou Inst Chem Phys, Key Lab Solid Lubricat, Beijing 100864, Peoples R China
Recommended Citation
GB/T 7714
Zhu HT,Wang, Li-Jing,Ji KG,et al. Synthesis of 3,4-Dihalogenated Furan-2-(5H)-ones by Electrophilic Cyclization of 4-Hydroxy-2-alkynoates[J]. Chemistry - An Asian Journal,2012,7(8):1862-1866.
APA Zhu HT,Wang, Li-Jing,Ji KG,Liu XY,Liang YM,&梁永民.(2012).Synthesis of 3,4-Dihalogenated Furan-2-(5H)-ones by Electrophilic Cyclization of 4-Hydroxy-2-alkynoates.Chemistry - An Asian Journal,7(8),1862-1866.
MLA Zhu HT,et al."Synthesis of 3,4-Dihalogenated Furan-2-(5H)-ones by Electrophilic Cyclization of 4-Hydroxy-2-alkynoates".Chemistry - An Asian Journal 7.8(2012):1862-1866.
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