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Organic and Biomolecular Chemistry

Volumn 12, Issue 2, 2014, Pages 307-315

The acid-catalysed synthesis of 7-azaindoles from 3-alkynyl-2- aminopyridines and their antimicrobial activity

(4) Leboho, Tlabo C a Van Vuuren, Sandy F b Michael, Joseph P a De Koning, Charles B a

a UNIVERSITY OF THE WITWATERSRAND (South Africa)

b UNIVERSITY OF THE WITWATERSRAND (South Africa)

Author keywords

[No Author keywords available]

Indexed keywords

ACIDIC CONDITIONS; AMINOPYRIDINES; ANTI-MICROBIAL ACTIVITY; CRYPTOCOCCUS NEOFORMANS; TRIFLUOROACETIC ANHYDRIDES;

CHEMISTRY; POSITIVE IONS;

YEAST;

7 AZAINDOLE DIMER; 7-AZAINDOLE DIMER; ACID; AMINOPYRIDINE DERIVATIVE; ANTIFUNGAL AGENT; ANTIINFECTIVE AGENT; INDOLE DERIVATIVE;

ARTICLE; BACTERIUM; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; DOSE RESPONSE; DRUG EFFECT; FUNGUS; MICROBIAL SENSITIVITY TEST; STRUCTURE ACTIVITY RELATION; SYNTHESIS;

ACIDS; AMINOPYRIDINES; ANTI-BACTERIAL AGENTS; ANTIFUNGAL AGENTS; BACTERIA; CATALYSIS; DOSE-RESPONSE RELATIONSHIP, DRUG; FUNGI; INDOLES; MICROBIAL SENSITIVITY TESTS; MOLECULAR STRUCTURE; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 84889834022 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c3ob41798k Document Type: Article

Times cited : (37)

References (30)

1
- 67650665029
- S. R. Walker E. J. Carter B. C. Huff J. C. Morris Chem. Rev. 2009 109 3080 3098
- (2009) Chem. Rev. , vol.109 , pp. 3080-3098
- Walker, S.R.¹ Carter, E.J.² Huff, B.C.³ Morris, J.C.⁴

2
- 0037294445
- M. Prudhomme Eur. J. Med. Chem. 2003 38 123 140
- (2003) Eur. J. Med. Chem. , vol.38 , pp. 123-140
- Prudhomme, M.¹

3
- 84862569941
- B. Nowicka-Sans Y.-F. Gong B. McAuliffe I. Dicker H.-T. Ho N. Zhou B. Eggers P.-F. Lin N. Ray M. Wind-Rotolo L. Zhu A. Majumdar D. Stock M. Lataillade G. J. Hanna J. D. Matiskella Y. Ueda T. Wang J. F. Kadow N. A. Meanwell M. Krystal Antimicrob. Agents Chemother. 2012 56 3498 3507
- (2012) Antimicrob. Agents Chemother. , vol.56 , pp. 3498-3507
- Nowicka-Sans, B.¹ Gong, Y.-F.² McAuliffe, B.³ Dicker, I.⁴ Ho, H.-T.⁵ Zhou, N.⁶ Eggers, B.⁷ Lin, P.-F.⁸ Ray, N.⁹ Wind-Rotolo, M.¹⁰ Zhu, L.¹¹ Majumdar, A.¹² Stock, D.¹³ Lataillade, M.¹⁴ Hanna, G.J.¹⁵ Matiskella, J.D.¹⁶ Ueda, Y.¹⁷ Wang, T.¹⁸ Kadow, J.F.¹⁹ Meanwell, N.A.²⁰ Krystal, M.²¹ more..

4
- 84877579678
- J. Y. Mérour S. Routier F. Suzenet B. Joseph Tetrahedron 2013 69 4767 4834
- (2013) Tetrahedron , vol.69 , pp. 4767-4834
- Mérour, J.Y.¹ Routier, S.² Suzenet, F.³ Joseph, B.⁴

5
- 34250678785
- J. J. Song J. T. Reeves F. Gallou Z. Tan N. K. Yee C. H. Senanayake Chem. Soc. Rev. 2007 36 1120 1132
- (2007) Chem. Soc. Rev. , vol.36 , pp. 1120-1132
- Song, J.J.¹ Reeves, J.T.² Gallou, F.³ Tan, Z.⁴ Yee, N.K.⁵ Senanayake, C.H.⁶

6
- 0037997585
- J.-Y. Mérour B. Joseph Curr. Org. Chem. 2001 5 471 506
- (2001) Curr. Org. Chem. , vol.5 , pp. 471-506
- Mérour, J.-Y.¹ Joseph, B.²

7
- 33845786925
- F. Popowycz S. Routier B. Joseph J.-Y. Mérour Tetrahedron 2007 63 1031 1064
- (2007) Tetrahedron , vol.63 , pp. 1031-1064
- Popowycz, F.¹ Routier, S.² Joseph, B.³ Mérour, J.-Y.⁴

8
- 34547183435
- M. C. de Mattos S. Alatorre-Santamaría V. Gotor-Fernández V. Gotor Synthesis 2007 2149 2152
- (2007) Synthesis , pp. 2149-2152
- De Mattos, M.C.¹ Alatorre-Santamaría, S.² Gotor-Fernández, V.³ Gotor, V.⁴

9
- 0037463514
- C. Koradin W. Dohle A. L. Rodriguez B. Schmid P. Knochel Tetrahedron 2003 59 1571 1587
- (2003) Tetrahedron , vol.59 , pp. 1571-1587
- Koradin, C.¹ Dohle, W.² Rodriguez, A.L.³ Schmid, B.⁴ Knochel, P.⁵

10
- 33746901222
- M. McLaughlin M. Palucki I. W. Davies Org. Lett. 2006 8 3307 3310
- (2006) Org. Lett. , vol.8 , pp. 3307-3310
- McLaughlin, M.¹ Palucki, M.² Davies, I.W.³

11
- 0034679471
- A. L. Rodriguez C. Koradin W. Dohle P. Knochel Angew. Chem., Int. Ed. 2000 39 2488 2490
- (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 2488-2490
- Rodriguez, A.L.¹ Koradin, C.² Dohle, W.³ Knochel, P.⁴

12
- 29744431958
- C. Harcken Y. Ward D. Thomson D. Riether Synlett 2005 3121 3125
- (2005) Synlett , pp. 3121-3125
- Harcken, C.¹ Ward, Y.² Thomson, D.³ Riether, D.⁴

13
- 34548202736
- K. C. Majumdar S. Mondal Tetrahedron Lett. 2007 48 6951 6953
- (2007) Tetrahedron Lett. , vol.48 , pp. 6951-6953
- Majumdar, K.C.¹ Mondal, S.²

14
- 26844432326
- S. E. Pearson S. Nandan Synthesis 2005 2503 2506
- (2005) Synthesis , pp. 2503-2506
- Pearson, S.E.¹ Nandan, S.²

15
- 44949172674
- N. Sakai N. Annaka A. Fujita A. Sato T. Konakahara J. Org. Chem. 2008 73 4160 4165
- (2008) J. Org. Chem. , vol.73 , pp. 4160-4165
- Sakai, N.¹ Annaka, N.² Fujita, A.³ Sato, A.⁴ Konakahara, T.⁵

16
- 54449084864
- K. C. Majumdar S. Samanta B. Chattopadhyay Tetrahedron Lett. 2008 49 7213 7216
- (2008) Tetrahedron Lett. , vol.49 , pp. 7213-7216
- Majumdar, K.C.¹ Samanta, S.² Chattopadhyay, B.³

17
- 22844433807
- S. Cacchi G. Fabrizi L. M. Parisi J. Comb. Chem. 2005 7 510 512
- (2005) J. Comb. Chem. , vol.7 , pp. 510-512
- Cacchi, S.¹ Fabrizi, G.² Parisi, L.M.³

18
- 70350018332
- A. Carpita A. Ribecai Tetrahedron Lett. 2009 50 6877 6881
- (2009) Tetrahedron Lett. , vol.50 , pp. 6877-6881
- Carpita, A.¹ Ribecai, A.²

19
- 77955420796
- A. Carpita A. Ribecai P. Stabile Tetrahedron 2010 66 7169 7178
- (2010) Tetrahedron , vol.66 , pp. 7169-7178
- Carpita, A.¹ Ribecai, A.² Stabile, P.³

20
- 68349135119
- T. C. Leboho J. P. Michael W. A. L. van Otterlo S. F. van Vuuren C. B. de Koning Bioorg. Med. Chem. Lett. 2009 19 4948 4951
- (2009) Bioorg. Med. Chem. Lett. , vol.19 , pp. 4948-4951
- Leboho, T.C.¹ Michael, J.P.² Van Otterlo, W.A.L.³ Van Vuuren, S.F.⁴ De Koning, C.B.⁵

21
- 84857368544
- L. V. Politanskaya I. P. Chuikov E. A. Kolodina M. S. Shvartsberg V. D. Shteingarts J. Fluorine Chem. 2012 135 97 107
- (2012) J. Fluorine Chem. , vol.135 , pp. 97-107
- Politanskaya, L.V.¹ Chuikov, I.P.² Kolodina, E.A.³ Shvartsberg, M.S.⁴ Shteingarts, V.D.⁵

22
- 58149131315
- K. Venkateswarlu K. Suneel B. Das K. N. Reddy T. S. Reddy Synth. Commun. 2009 39 215 219
- (2009) Synth. Commun. , vol.39 , pp. 215-219
- Venkateswarlu, K.¹ Suneel, K.² Das, B.³ Reddy, K.N.⁴ Reddy, T.S.⁵

23
- 84859981574
- K. Kumaran M. K. S. Raja K. R. Jaisankar Int. J. PharmTech Res. 2012 4 169 175
- (2012) Int. J. PharmTech Res. , vol.4 , pp. 169-175
- Kumaran, K.¹ Raja, M.K.S.² Jaisankar, K.R.³

24
- 34250335109
- N. Lebouvier F. Pagniez M. Duflos P. Le Pape Y. M. Na G. Le Baut M. Le Borgne Bioorg. Med. Chem. Lett. 2007 17 3686 3689
- (2007) Bioorg. Med. Chem. Lett. , vol.17 , pp. 3686-3689
- Lebouvier, N.¹ Pagniez, F.² Duflos, M.³ Le Pape, P.⁴ Na, Y.M.⁵ Le Baut, G.⁶ Le Borgne, M.⁷

25
- 84878322313
- R. M. La Hoz P. G. Pappas Drugs 2013 73 495 504
- (2013) Drugs , vol.73 , pp. 495-504
- La Hoz, R.M.¹ Pappas, P.G.²

26
- 84872699143
- Y. Liao M. Chen T. Hartmann R. Y. Yang W. Q. Liao Chin. Med. J. 2013 126 361 368
- (2013) Chin. Med. J. , vol.126 , pp. 361-368
- Liao, Y.¹ Chen, M.² Hartmann, T.³ Yang, R.Y.⁴ Liao, W.Q.⁵

27
- 0035899182
- H.-R. Tsou N. Mamuya B. D. Johnson M. F. Reich B. C. Gruber F. Ye R. Nilakantan R. Shen C. Discafani R. DeBlanc R. Davis F. E. Koehn L. M. Greenberger Y.-F. Wang A. Wissner J. Med. Chem. 2001 44 2719 2734
- (2001) J. Med. Chem. , vol.44 , pp. 2719-2734
- Tsou, H.-R.¹ Mamuya, N.² Johnson, B.D.³ Reich, M.F.⁴ Gruber, B.C.⁵ Ye, F.⁶ Nilakantan, R.⁷ Shen, R.⁸ Discafani, C.⁹ Deblanc, R.¹⁰ Davis, R.¹¹ Koehn, F.E.¹² Greenberger, L.M.¹³ Wang, Y.-F.¹⁴ Wissner, A.¹⁵

28
- 77954548244
- G. Acquaah-Harrison S. Zhou J. V. Hines S. C. Bergmeier J. Comb. Chem. 2010 12 491 496
- (2010) J. Comb. Chem. , vol.12 , pp. 491-496
- Acquaah-Harrison, G.¹ Zhou, S.² Hines, J.V.³ Bergmeier, S.C.⁴

29
- 84889776643
- WO 2011137022 A1, 3 November 2011
- B. Cash, C. Fischer, Y. Garcia, J. Jung, J. Katz, J. Kim, A. Rivkin, A. Schell, T. Siu, D. Witter and H. Zhou, Azaindoles as janus kinase inhibitors, WO 2011137022 A1, 2011, 3 November 2011
- (2011) Azaindoles as Janus Kinase Inhibitors
- Cash, B.¹ Fischer, C.² Garcia, Y.³ Jung, J.⁴ Katz, J.⁵ Kim, J.⁶ Rivkin, A.⁷ Schell, A.⁸ Siu, T.⁹ Witter, D.¹⁰ Zhou, H.¹¹

30
- 33645753921
- Clsi Clinical And Laboratory Standards Institute Approved Standard M100-S22, National Committee for Clinical Laboratory Standards, Fort Wayne, Ind, USA, 22nd edn
- CLSI, Clinical and Laboratory Standards Institute, Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically, Approved Standard M100-S22, National Committee for Clinical Laboratory Standards, Fort Wayne, Ind, USA, 22nd edn, 2012
- (2012) Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria That Grow Aerobically

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