Antimony(III) sulfate catalyzed condensation reaction of indoles with carbonyl compounds

Monatshefte fur Chemie

Volumn 139, Issue 2, 2008, Pages 111-115

  Srinivasa, Aswathanarayana ^a   Varma, Putta Prabhakar ^a   Hulikal, Vijaykumar ^b   Mahadevan, Kittappa M ^a  

^a KUVEMPU UNIVERSITY   (India)

^b BioOrganics & Applied Materials Pvt Ltd   (India)

Author keywords

3 Indolyl ketones; Aldehydes; Antimony sulfate; Bis(indolyl)methanes; Indoles

Indexed keywords

EID: 38949096879     PISSN: 00269247     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00706-007-0697-z     Document Type: Article

References (43)

1. T Osawa M Namiki 1983 Tetrahedron Lett 24 4719
2. JK Porter CW Bacon JD Robbin DS Himmelsbach HC Higman 1977 J Agric Food Chem 25 88
3. TR Garbe M Kobayashi N Shimizu N Takesue M Ozawa H Yukawa 2000 J Nat Prod 63 596
4. C Hong GL Firestone LF Bjeldanes 2002 Biochem Pharmacol 63 1085
5. A Kamal A Qureshi 1963 Tetrahedron 19 513
6. BV Gregorovich K Liang M Clugston S Macdonald 1968 Can J Chem 46 3291
7. M Roomi S Macdonald 1970 Can J Chem 48 139
8. M Auria 1991 Tetrahedron 47 9225
9. RS Pankajkumar US Devendrapratap DS Shriniwas 2005 Synth Commun 35 2133
10. A Chatterjee S Manna J Benerji C Pascard T Prange J Sghoolery 1980 J Chem Soc Perkin Trans 1 553
11. G Babu N Sridhar PT Perumal 2000 Synth Commun 30 1609
12. Yadav JS, Reddy BVS, Murthy VSR, Kumar GM, Madan C (2003) Synthesis 783
13. M Xia S-B Wang W-B Yuan 2004 Synth Commun 34 3175
14. RR Nagawade DB Shinde 2005 Bull Korean Chem Soc 26 1962
15. L-P Mo Z-C Ma Z-H Zhang 2005 Synth Commun 35 1997
16. BP Bandagar SV Bettigeri NS Joshi 2004 Monatsh Chem 135 1265
17. Sharma GVM, Reddy JJ, Lakshmi PS, Krishna PR (2004) 45: 7729
18. R Nagarajan PT Perumal 2004 Synth Commun 32 105
19. R Nagarajan PT Perumal 2004 Chem Lett 33 288
20. BP Bandgar KA Shaikh 2003 Tetrahedron Lett 44 1959
21. X-L Feng C-J Guan C-X Zhao 2004 Synth Commun 34 487
22. H Koshima W Matsuaka 2002 J Heterocyclic Chem 39 1089
23. C Ramesh J Baneree R Pal B Das 2003 Adv Synth Catal 345 557
24. M Chakrabarty N Ghosh R Basak Y Harigaya 1996 Tetrahedron Lett 37 4467
25. JS Yadav BVS Reddy S Sunitha 2003 Adv Synth Catal 345 349
26. L Wang J Han H Tian J Sheng Z Fan X Tung 2005 Synlett 2 337
27. X-L Mi S-Z Luo J-Q He J-P Cheng 2004 Tetrahedron Lett 45 4567
28. D Chen L Yu PG Wang 1996 Tetrahedron Lett 37 4467
29. S Samajdar FF Becker BK Banik 2000 Tetrahedron Lett 41 8017
30. S Samajdar FF Becker BK Banik 2002 Synth Commun 32 1917
31. N Srivastava BK Banik 2003 J Org Chem 68 2109
32. GA Olah J Nishimura 1974 J Am Chem Soc 16 2214
33. J Szmuskovicz 1957 J Am Chem Soc 79 2819
34. J Christofers 1998 Eur J Org Chem 1259 9
35. LR Babu PT Perumal 2000 Aldricchim Acta 33 16
36. K Manabe Y Mori T Wkabayashi S Nagayama S Kobayashi 2000 J Am Chem Soc 122 7202
37. G Bartoli M Bartolacci M Bosco G Foglia A Giuliani E Marcantoni L Sambari E Torregiani 2003 J Org Chem 68 4594
38. N Srivastava BK Banik 2003 J Org Chem 68 2109
39. DU Singh PR Singh SD Samant 2006 Synth Commun 36 1265
40. H-B Zhang L Liu Y-L Liu Y-J Chen J Wang D Wang 2007 Synth Commun 37 173
41. M Bandini GP Cozzi M Glacomini P Melchiorre S Selva A Umani-Ronchi 2002 J Org Chem 67 3700
42. HJ Poupaert J Bukuru A Gozzo 1999 Monatsh Chem 130 929
43. RJ Sunberg 1996 The Chem of Indoles Academic Press New York 113