Palladium-Catalyzed Divergent Reactions of 1,6-Enyne Carbonates: Synthesis of Vinylidenepyridines and Vinylidenepyrrolidines | |
Department | 固体润滑国家重点实验室 |
Zhao SC(赵树春)1; Ji KG(纪克攻)1; Lu, Lei1; He, Ting1; Zhou, An-Xi1; Yan, Ru-Long1; Ali, Shaukat1; Liu XY(刘雪原)1; Liang YM(梁永民)1,2; Liang YM(梁永民) | |
2012 | |
Source Publication | Journal of Organic Chemistry |
ISSN | 0022-3263 |
Volume | 77Issue:6Pages:2763-2772 |
Abstract | A method for preparing five- or six-membered heterocyclic compounds from enyne carbonates via palladium catalysis was developed. Enyne carbonates were transformed into 3-vinylidene-1-tosylpyridines 2 in the presence of PdI2 as the catalyst. Using Pd(dba)2 as the catalyst, 3-vinylidene-1-tosylpyrrolidines 3 were obtained. Further functionalizations of compounds 3 were carried out in a one-pot manner. |
Subject Area | 材料科学与物理化学 |
DOI | 10.1021/jo202590w |
Funding Organization | the NSF (NSF-21072080;NSF-20732002);National Basic Research Program of China (973 program) 2010CB833203;the 111 Project |
Indexed By | SCI |
If | 4.564 |
Language | 英语 |
compositor | 第二作者单位 |
Citation statistics | |
Document Type | 期刊论文 |
Identifier | http://ir.licp.cn/handle/362003/19429 |
Collection | 固体润滑国家重点实验室(LSL) |
Corresponding Author | Liang YM(梁永民) |
Affiliation | 1.Lanzhou Univ, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China 2.Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Solid Lubricat, Lanzhou 730000, Peoples R China |
Recommended Citation GB/T 7714 | Zhao SC,Ji KG,Lu, Lei,et al. Palladium-Catalyzed Divergent Reactions of 1,6-Enyne Carbonates: Synthesis of Vinylidenepyridines and Vinylidenepyrrolidines[J]. Journal of Organic Chemistry,2012,77(6):2763-2772. |
APA | Zhao SC.,Ji KG.,Lu, Lei.,He, Ting.,Zhou, An-Xi.,...&梁永民.(2012).Palladium-Catalyzed Divergent Reactions of 1,6-Enyne Carbonates: Synthesis of Vinylidenepyridines and Vinylidenepyrrolidines.Journal of Organic Chemistry,77(6),2763-2772. |
MLA | Zhao SC,et al."Palladium-Catalyzed Divergent Reactions of 1,6-Enyne Carbonates: Synthesis of Vinylidenepyridines and Vinylidenepyrrolidines".Journal of Organic Chemistry 77.6(2012):2763-2772. |
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