LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Cobalt-Catalyzed Dimerization and Homocoupling of Terminal Alkynes
DepartmentOSSO国家重点实验室
Xu Daqian1; Sun Qiangsheng2; Quan Zhengjun1; Wang Xicun1; Sun Wei2
2018
Source PublicationAsian Journal of Organic Chemistry
ISSN2193-5807
Volume7Issue:1Pages:155-159
Abstract

Methods toward the dimerization and homocoupling of terminal alkynes have been established that employ Co complexes along with tBuOK under different atmosphere. A variety of Z‐1,3‐enynes were furnished with a high Z:E (up to 93:7) ratio in moderate to very good yields under inert atmosphere. Alternatively, the Glaser homocoupling reaction of terminal alkynes was also accomplished with a Co catalyst, successfully affording various 1,3‐diynes in excellent yields (up to 93 %) under oxygen.

KeywordAlkynes Cobalt Dimerization Homocoupling
Subject Area物理化学与绿色催化
DOI10.1002/ajoc.201700587
Funding Organizationthe National Natural Science Foundation of China (21473226 ; 21362031)
Indexed BySCI
If2.496
Language英语
Funding Project仿生与生物催化研究组
compositor第二作者单位
Citation statistics
Cited Times:25[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/23767
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding AuthorWang Xicun; Sun Wei
Affiliation1.College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou 730070, Gansu (China)
2.State Key Laboratory for Oxo Synthesis and Selective Oxidation Chinese Academy of Sciences, Lanzhou 730000 (China)
Recommended Citation
GB/T 7714
Xu Daqian,Sun Qiangsheng,Quan Zhengjun,et al. Cobalt-Catalyzed Dimerization and Homocoupling of Terminal Alkynes[J]. Asian Journal of Organic Chemistry,2018,7(1):155-159.
APA Xu Daqian,Sun Qiangsheng,Quan Zhengjun,Wang Xicun,&Sun Wei.(2018).Cobalt-Catalyzed Dimerization and Homocoupling of Terminal Alkynes.Asian Journal of Organic Chemistry,7(1),155-159.
MLA Xu Daqian,et al."Cobalt-Catalyzed Dimerization and Homocoupling of Terminal Alkynes".Asian Journal of Organic Chemistry 7.1(2018):155-159.
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