AlCl3 mediated unexpected migration of sulfonyl groups: Regioselective synthesis of 7-sulfonyl indoles of potential pharmacological interest

Chemical Communications

Volumn 48, Issue 84, 2012, Pages 10434-10436

  Prasad, Bagineni ^a   Adepu, Raju ^a   Sandra, Sandhya ^a   Rambabu, D ^a   Krishna, G Rama ^b   Reddy, C Malla ^b   Deora, Girdhar Singh ^a   Misra, Parimal ^a   Pal, Manojit ^a  

^a UNIVERSITY OF HYDERABAD   (India)

^b INDIAN INSTITUTE OF SCIENCE EDUCATION AND RESEARCH KOLKATA   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ALUMINUM CHLORIDE; CHORISMATE MUTASE; ENZYME INHIBITOR; INDOLE DERIVATIVE; ALUMINUM DERIVATIVE; CHLORIDE; SULFONE;

ARTICLE; DRUG SYNTHESIS; MYCOBACTERIUM TUBERCULOSIS; NONHUMAN; STEREOCHEMISTRY; CHEMICAL STRUCTURE; CHEMISTRY; DRUG ANTAGONISM; ENZYMOLOGY; METABOLISM; STEREOISOMERISM; STRUCTURE ACTIVITY RELATION; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

ALUMINUM COMPOUNDS; CHLORIDES; CHORISMATE MUTASE; CRYSTALLOGRAPHY, X-RAY; ENZYME INHIBITORS; INDOLES; MODELS, MOLECULAR; MOLECULAR STRUCTURE; MYCOBACTERIUM TUBERCULOSIS; STEREOISOMERISM; STRUCTURE-ACTIVITY RELATIONSHIP; SULFONES;

EID: 84866893348     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c2cc35757g     Document Type: Article

References (15)

1. G. R. Humphrey, J. T. Kuethe, Chem. Rev, 2006, 106, 2875
2. S. Cacchi, G. Fabrizi, Chem. Rev, 2005, 105, 2873
3. G. W. Gribble, in Comprehensive Heterocyclic Chemistry II, ed. A. R. Katrizky, C. W. Rees and E. F. V. Scriven, Pergamon, Oxford, 1996, vol. 2, p. 20
4. E. Haslam, Shikimic Acid: Metabolism and Metabolites, Wiley, New York, 1993
5. H. Agarwal, A. Kumar, N. C. Bal, M. I. Siddiqi, A. Arora, Bioorg. Med. Chem. Lett, 2007, 17, 3053
6. A. Nakhi, B. Prasad, R. M. Rao, U. Reddy, S. Sandra, R. Kapavarapu, D. Rambabu, G. R. Krishna, C. M. Reddy, R. Kishore, P. Misra, J. Iqbal, M. Pal, MedChemComm, 2011, 2, 1006
7. K. S. Kumar, D. Rambabu, S. Sandra, R. Kapavarapu, G. R. Krishna, M. V. B. Rao, K. Chatti, C. M. Reddy, P. Misra, M. Pal, Bioorg. Med. Chem, 2012, 20, 1711
8. K. S. Kumar, R. Adepu, S. Sandra, D. Rambabu, G. R. Krishna, C. M. Reddy, P. Misra, M. Pal, Bioorg. Med. Chem. Lett, 2012, 22, 1146
9. T. R. Reddy, L. S. Reddy, G. R. Reddy, K. Yarbagi, Y. Lingappa, D. Rambabu, G. R. Krishna, C. M. Reddy, K. S. Kumar, M. Pal, Green Chem, 2012, 14, 1870
10. X. Xin, D. Wang, X. Li, B. Wan, Angew. Chem, Int. Ed, 2012, 57, 1693
11. I. Nakamura, U. Yamagishi, D. Song, S. Konta, Y. Yamamoto, Angew. Chem, Int. Ed, 2007, 46, 2284
12. X. Hong, J. M. M. Oneto, S. France, A. Padwa, Tetrahedron Lett, 2006, 47, 2409
13. M. Pal, Synlett, 2009, 2896
14. S. K. Kim, S. K. Reddy, B. C. Nelson, G. B. Vasquez, A. Davis, A. J. Howard, S. Patterson, G. L. Gilliland, J. E. Ladner, P. T. Reddy, J. Bacteriol, 2006, 188, 8638
15. S. Sasso, C. Ramakrishnan, M. Gamper, D. Hilvert, P. Kast, FEBS J, 2005, 272, 375