Rhodium(II)-catalyzed intermolecular [3+2] annulation of N-vinyl indoles with N-tosyl-1,2,3-triazoles via an aza-vinyl Rh carbene

被引:17
作者
Jiang, Bo [1 ]
Shi, Min [1 ,2 ,3 ]
机构
[1] Univ Chinese Acad Sci, Shanghai Inst Organ Chem, Chinese Acad Sci, State Key Lab Organometall Chem, 345 Lingling Rd, Shanghai 200032, Peoples R China
[2] Nankai Univ, State Key Lab, Tianjin 300071, Peoples R China
[3] Nankai Univ, Inst Elementoorgan Chem, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
RHODIUM-CATALYZED TRANSANNULATION; TERMINAL ALKYNES; AZAVINYL CARBENES; SULFONYL AZIDES; ONE-POT; TETHERED N-SULFONYL-1,2,3-TRIAZOLES; INTRAMOLECULAR ANNULATION; POLYSUBSTITUTED PYRROLES; H FUNCTIONALIZATION; DIVERGENT SYNTHESIS;
D O I
10.1039/c7qo00703e
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The rhodium(II)-catalyzed annulations of N-vinyl indole derivatives and N-tosyl-1,2,3-triazoles have been developed in this paper, providing a convenient, efficient and straightforward access to synthesize indoles containing a N-dihydropyrrole in moderate to good yields. Furthermore, the reaction of N-vinyl indoles with 2.5 equiv. of N-tosyl-1,2,3-triazoles gave C3-functionalized indoles containing a N-dihydropyrrole in moderate yields after reduction with NaBH3CN in a one-pot manner. This finding gives a new synthetic protocol for the preparation of indoles containing a N-dihydropyrrole under mild conditions.
引用
收藏
页码:2459 / 2464
页数:6
相关论文
共 89 条
[31]   A multicomponent pathway-inspired regioselective synthesis of 2,3,4-trisubstituted 1H-pyrroles via [3+2] cycloaddition reaction [J].
Kalmode, Hanuman P. ;
Vadagaonkar, Kamlesh S. ;
Murugan, Kaliyappan ;
Chaskar, Atul C. .
NEW JOURNAL OF CHEMISTRY, 2015, 39 (06) :4631-4639
[32]   Synthesis of Pyrroles from Terminal Alkynes, N-Sulfonyl Azides, and Alkenyl Alkyl Ethers through 1-Sulfonyl-1,2,3-triazoles [J].
Kim, Cheol-Eui ;
Park, Sangjune ;
Eom, Dahan ;
Seo, Boram ;
Lee, Phil Ho .
ORGANIC LETTERS, 2014, 16 (07) :1900-1903
[33]   Biogenetically-Inspired Total Synthesis of Epidithiodiketopiperazines and Related Alkaloids [J].
Kim, Justin ;
Movassaghi, Mohammad .
ACCOUNTS OF CHEMICAL RESEARCH, 2015, 48 (04) :1159-1171
[34]  
Knorr L., 1884, Ber, V17, P2863, DOI [10.1002/cber.188401702254, DOI 10.1002/CBER.188401702254]
[35]  
Kobayashi J.i., 1992, The Alkaloids: Chemistry and Pharmacology, V41, P41
[36]   Marine Indole Alkaloids: Potential New Drug Leads for the Control of Depression and Anxiety [J].
Kochanowska-Karamyan, Anna J. ;
Hamann, Mark T. .
CHEMICAL REVIEWS, 2010, 110 (08) :4489-4497
[37]   Enantioselective Intermolecular C-H Functionalization of Allylic and Benzylic sp3 C-H Bonds Using N-Sulfonyl-1,2,3-triazoles [J].
Kubiak, Robert W., II ;
Mighion, Jeffrey D. ;
Wilkerson-Hill, Sidney M. ;
Alford, Joshua S. ;
Yoshidomi, Tetsushi ;
Davies, Huw M. L. .
ORGANIC LETTERS, 2016, 18 (13) :3118-3121
[38]   Rhodium Thiavinyl Carbenes from 1,2,3-Thiadiazoles Enable Modular Synthesis of Multisubstituted Thiophenes [J].
Kurandina, Dania ;
Gevorgyan, Vladimir .
ORGANIC LETTERS, 2016, 18 (08) :1804-1807
[39]   Catalytic Asymmetric Transannulation of NH-1,2,3-Triazoles with Olefins [J].
Kwok, Sen Wai ;
Zhang, Li ;
Grimster, Neil P. ;
Fokin, Valery V. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2014, 53 (13) :3452-3456
[40]   Synthetic Approaches to 3-(2-Nitroalkyl) Indoles and Their Use to Access Tryptamines and Related Bioactive Compounds [J].
Lancianesi, Stefano ;
Palmieri, Alessandro ;
Petrini, Marino .
CHEMICAL REVIEWS, 2014, 114 (14) :7108-7149