SCOPUS 정보 검색 플랫폼

Canadian Journal of Chemistry

Volumn 90, Issue 2, 2012, Pages 214-221

Synthesis of 2,3,4-trisubstituted pyrroles via a facile reaction of vinyl azides and tosylmethyl isocyanide

(5) Chen, Wenteng a Shao, Jiaan a Li, Zhi a Giulianotti, Marc A b Yu, Yongping a,b

a ZHEJIANG UNIVERSITY (China)

b TORREY PINES INSTITUTE FOR MOLECULAR STUDIES (United States)

Author keywords

2,3,4 trisubstituted pyrroles; Cyclization reaction; Multicomponent reaction; Nucleophilic reaction; Vinyl azides

Indexed keywords

2,3,4-TRISUBSTITUTED PYRROLES; CYCLIZATION REACTION; MULTI-COMPONENT REACTIONS; NUCLEOPHILIC REACTION; VINYL AZIDES;

CYANIDES; POTASSIUM COMPOUNDS; SYNTHESIS (CHEMICAL);

CYCLIZATION;

EID: 84863056439 PISSN: 00084042 EISSN: None Source Type: Journal
DOI: 10.1139/v11-150 Document Type: Article

Times cited : (20)

References (24)

1
- 24944474895
- Versatile direct synthesis of oligosubstituted pyrroles by cycloaddition of α-metalated isocyanides to acetylenes
- DOI 10.1002/anie.200502140
- a Larionov O. V. de Meijere A. Angew. Chem. Int. Ed. 2005, 44 (35), 5664. 10.1002/anie.200502140 (Pubitemid 41312149)
- (2005) Angewandte Chemie - International Edition , vol.44 , Issue.35 , pp. 5664-5667
- Larionov, O.V.¹ De Meijere, A.²

2
- 0037015447
- 10.1021/ol0267073
- b Smith N. D. Huang D. Cosford N. D. P. Org. Lett. 2002, 4 (20), 3537. 10.1021/ol0267073
- (2002) Org. Lett. , vol.4 , Issue.20 , pp. 3537
- Smith, N.D.¹ Huang, D.² Cosford, N.D.P.³

3
- 0037435063
- Simple, potent, and selective pyrrole inhibitors of monoamine oxidase types A and B
- DOI 10.1021/jm0256124
- a Silvestri R. La Regina G. De Martino G. Artico M. Befani O. Palumbo M. Agostinelli E. Turini P. J. Med. Chem. 2003, 46 (6), 917. 10.1021/jm0256124 (Pubitemid 36423138)
- (2003) Journal of Medicinal Chemistry , vol.46 , Issue.6 , pp. 917-920
- Silvestri, R.¹ La Regina, G.² De Martino, G.³ Artico, M.⁴ Befani, O.⁵ Palumbo, M.⁶ Agostinelli, E.⁷ Turini, P.⁸

4
- 39149095977
- Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high throughput screening assay. 4. Structure-activity relationships of N-alkyl substituted pyrrole fused at the 7,8-positions
- DOI 10.1021/jm7010657
- b Kemnitzer W. Drewe J. Jiang S. Zhang H. Crogan-Grundy C. Labreque D. Bubenick M. Attardo G. Denis R. Lamothe S. Gourdeau H. Tseng B. Kasibhatla S. Cai S. X. J. Med. Chem. 2008, 51 (3), 417. 10.1021/jm7010657 (Pubitemid 351252270)
- (2008) Journal of Medicinal Chemistry , vol.51 , Issue.3 , pp. 417-423
- Kemnitzer, W.¹ Drewe, J.² Jiang, S.³ Zhang, H.⁴ Crogan-Grundy, C.⁵ Labreque, D.⁶ Bubenick, M.⁷ Attardo, G.⁸ Denis, R.⁹ Lamothe, S.¹⁰ Gourdeau, H.¹¹ Tseng, B.¹² Kasibhatla, S.¹³ Sui, X.C.¹⁴

5
- 77249106011
- 10.1021/jm901216v
- c Pacorel B. Leung S. C. Stachulski A. V. Davies J. Vivas L. Lander H. Ward S. A. Kaiser M. Brun R. ONeill P. M. J. Med. Chem. 2010, 53 (2), 633. 10.1021/jm901216v
- (2010) J. Med. Chem. , vol.53 , Issue.2 , pp. 633
- Pacorel, B.¹ Leung, S.C.² Stachulski, A.V.³ Davies, J.⁴ Vivas, L.⁵ Lander, H.⁶ Ward, S.A.⁷ Kaiser, M.⁸ Brun, R.⁹ O'Neill, P.M.¹⁰

6
- 34250324205
- Dipyrrolyl-functionalized bipyridine-based anion receptors for emission-based selective detection of dihydrogen phosphate
- DOI 10.1002/chem.200601514
- d Plitt P. Gross D. E. Lynch V. M. Sessler J. L. Chemistry 2007, 13 (5), 1374. 10.1002/chem.200601514 (Pubitemid 46925450)
- (2007) Chemistry - A European Journal , vol.13 , Issue.5 , pp. 1374-1381
- Plitt, P.¹ Gross, D.E.² Lynch, V.M.³ Sessler, J.L.⁴

7
- 0035799160
- Regioselective alkylation reactions of hydrazones derived from phosphine oxides and phosphonates. Synthesis of phosphorus substituted 1-amino-pyrrolones, pyridinones and pyrroles
- DOI 10.1016/S0040-4020(01)00033-3, PII S0040402001000333
- Palacios F. Aparicio D. de los Santos J. M. Vicario J. Tetrahedron 2001, 57 (10), 1961. 10.1016/S0040-4020(01)00033-3 (Pubitemid 32178525)
- (2001) Tetrahedron , vol.57 , Issue.10 , pp. 1961-1972
- Palacios, F.¹ Aparicio, D.² De Los Santos, J.M.³ Vicario, J.⁴

8
- 3242695438
- Catalytic multicomponent synthesis of highly substituted pyrroles utilizing a one-pot sila-stetter/paal-knorr strategy
- DOI 10.1021/ol049044t
- Bharadwaj A. R. Scheidt K. A. Org. Lett. 2004, 6 (14), 2465. 10.1021/ol049044t (Pubitemid 38952564)
- (2004) Organic Letters , vol.6 , Issue.14 , pp. 2465-2468
- Bharadwaj, A.R.¹ Scheidt, K.A.²

9
- 11144250168
- Pyrrole syntheses by multicomponent coupling reactions
- DOI 10.1002/anie.200461073
- Balme G. Angew. Chem. Int. Ed. 2004, 43 (46), 6238. 10.1002/anie. 200461073 (Pubitemid 40029452)
- (2004) Angewandte Chemie - International Edition , vol.43 , Issue.46 , pp. 6238-6241
- Balme, G.¹

10
- 67650047702
- 10.1055/s-0028-1087991
- a Baxendale I. R. Buckle C. D. Ley S. V. Tamborini L. Synthesis 2009, 2009 (9), 1485. 10.1055/s-0028-1087991
- (2009) Synthesis , vol.2009 , Issue.9 , pp. 1485
- Baxendale, I.R.¹ Buckle, C.D.² Ley, S.V.³ Tamborini, L.⁴

11
- 0000238655
- 10.1021/jo00034a011
- b van Leusen D. van Echten E. van Leusen A. M. J. Org. Chem. 1992, 57 (8), 2245. 10.1021/jo00034a011
- (1992) J. Org. Chem. , vol.57 , Issue.8 , pp. 2245
- Van Leusen, D.¹ Van Echten, E.² Van Leusen, A.M.³

12
- 0000498308
- 10.1016/S0040-4039(01)85244-8
- c van Leusen A. M. Siderius H. Hoogenboom B. E. van Leusen D. Tetrahedron Lett. 1972, 13 (52), 5337. 10.1016/S0040-4039(01)85244-8
- (1972) Tetrahedron Lett. , vol.13 , Issue.52 , pp. 5337
- Van Leusen, A.M.¹ Siderius, H.² Hoogenboom, B.E.³ Van Leusen, D.⁴

13
- 37049163293
- 10.1039/ct9181300639
- Robinson G. M. Robinson R. J. Chem. Soc. Trans. 1918, 113, 639. 10.1039/ct9181300639
- (1918) J. Chem. Soc. Trans. , vol.113 , pp. 639
- Robinson, G.M.¹ Robinson, R.²

14
- 0035874693
- A novel synthesis of 2-aminopyrroles using a three-component reaction
- DOI 10.1021/jo001714v
- Nair V. Vinod A. U. Rajesh C. J. Org. Chem. 2001, 66 (12), 4427. 10.1021/jo001714v (Pubitemid 32867590)
- (2001) Journal of Organic Chemistry , vol.66 , Issue.12 , pp. 4427-4429
- Nair, V.¹ Vinod, A.U.² Rajesh, C.³

15
- 38749150358
- 10.1021/ol702727j
- a Chiba S. Wang Y.-F. Lapointe G. Narasaka K. Org. Lett. 2008, 10 (2), 313. 10.1021/ol702727j
- (2008) Org. Lett. , vol.10 , Issue.2 , pp. 313
- Chiba, S.¹ Wang, Y.-F.² Lapointe, G.³ Narasaka, K.⁴

16
- 58149157809
- 10.1021/ol802120u
- b Wang Y.-F. Toh K. K. Chiba S. Narasaka K. Org. Lett. 2008, 10 (21), 5019. 10.1021/ol802120u
- (2008) Org. Lett. , vol.10 , Issue.21 , pp. 5019
- Wang, Y.-F.¹ Toh, K.K.² Chiba, S.³ Narasaka, K.⁴

17
- 30044440260
- 10.1002/ejoc.200500387
- Minetto G. Raveglia L. F. Sega A. Taddei M. Eur. J. Org. Chem. 2005, 2005 (24), 5277. 10.1002/ejoc.200500387
- (2005) Eur. J. Org. Chem. , vol.2005 , Issue.24 , pp. 5277
- Minetto, G.¹ Raveglia, L.F.² Sega, A.³ Taddei, M.⁴

18
- 0000498308
- 10.1016/S0040-4039(01)85244-8
- a van Leusen A. M. Siderius H. Hoogenboom B. E. van Leusen D. Tetrahedron Lett. 1972, 13 (52), 5337. 10.1016/S0040-4039(01)85244-8
- (1972) Tetrahedron Lett. , vol.13 , Issue.52 , pp. 5337
- Van Leusen, A.M.¹ Siderius, H.² Hoogenboom, B.E.³ Van Leusen, D.⁴

19
- 0029920228
- 10.1055/s-1996-4306
- b ten Have R. Leusink F. R. van Leusen A. M. Synthesis 1996, 1996 (7), 871. 10.1055/s-1996-4306
- (1996) Synthesis , vol.1996 , Issue.7 , pp. 871
- Ten Have, R.¹ Leusink, F.R.² Van Leusen, A.M.³

20
- 0000109604
- 10.1021/jo972216y
- c Dijkstra H. P. ten Have R. van Leusen A. M. J. Org. Chem. 1998, 63 (16), 5332. 10.1021/jo972216y
- (1998) J. Org. Chem. , vol.63 , Issue.16 , pp. 5332
- Dijkstra, H.P.¹ Ten Have, R.² Van Leusen, A.M.³

21
- 77956208057
- 10.1021/ol101538x
- Chen W. Hu M. Wu J. Zou H. Yu Y. Org. Lett. 2010, 12 (17), 3863. 10.1021/ol101538x
- (2010) Org. Lett. , vol.12 , Issue.17 , pp. 3863
- Chen, W.¹ Hu, M.² Wu, J.³ Zou, H.⁴ Yu, Y.⁵

22
- 0037653954
- Gilchrist T. L. Mendonca R. ARKIVOC 2000, 1, 769.
- (2000) ARKIVOC , vol.1 , pp. 769
- Gilchrist, T.L.¹ Mendonca, R.²

23
- 2542509173
- 10.1002/1521-3773(20000915)39:18<3168: AID-ANIE3168>3.0.CO;2-U
- a Dömling A. Ugi I. Angew. Chem. Int. Ed. 2000, 39 (18), 3168. 10.1002/1521-3773(20000915)39:18<3168::AID-ANIE3168>3.0.CO;2-U
- (2000) Angew. Chem. Int. Ed. , vol.39 , Issue.18 , pp. 3168
- Dömling, A.¹ Ugi, I.²

24
- 79959907066
- 10.1002/anie.201006515
- b Ruijter E. Scheffelaar R. Orru R. V. A. Angew. Chem. Int. Ed. 2011, 50 (28), 6234. 10.1002/anie.201006515
- (2011) Angew. Chem. Int. Ed. , vol.50 , Issue.28 , pp. 6234
- Ruijter, E.¹ Scheffelaar, R.² Orru, R.V.A.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.