A facile, aqueous phase green synthetic protocol for the synthesis of 5,9b-dihydro-1H-[1,2,4]triazino[5,6-b]indole-3-ols/5,9b-dihydro-1H-[1,2,4] triazino[5,6-b]indole-3-thiols

Tetrahedron Letters

Volumn 52, Issue 37, 2011, Pages 4734-4737

  Ramesh, K ^a   Narayana Murthy, S ^a   Karnakar, K ^a   Nageswar, Y V D ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

Cyclodextrin; Isatin; Semicarbazide thiosemicarbazide; Water

Indexed keywords

5,9B DIHYDRO 1H [1,2,4]TRIAZINO[5,6 B]INDOLE 3 OL; 5,9B DIHYDRO1H [1,2,4]TRIAZINO[5,6 B]INDOLE 3 THIOL; ALPHA CYCLODEXTRIN; BETA CYCLODEXTRIN; GAMMA CYCLODEXTRIN; INDOLE DERIVATIVE; ISATIN; SEMICARBAZIDE; THIOSEMICARBAZIDE; UNCLASSIFIED DRUG; WATER;

AQUEOUS SOLUTION; ARTICLE; CATALYSIS; CATALYST; CONTROLLED STUDY; DRUG ACTIVITY; DRUG SYNTHESIS; RECYCLING;

EID: 80051695003     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.06.098     Document Type: Article

References (25)

1. C. Hansch, P.G. Sammes, and G.B. Taylor Comprehensive Medicinal Chemistry vol. 4 1990 Pergamon Oxford Chap 7.1
2. D.A. Erlanson, R.S. McDowell, and T.O. Brien J. Med. Chem. 47 2004 3463
3. S.G. Baginski, D.C. Pevear, M. Seipel, S.C.C. Sun, C.A. Benetatos, S.K. Chunduru, C.M. Rice, and M.S. Collett Proc. Natl. Acad. Sci. U.S.A. 97 2000 7981 7986
4. A. Padwa Prog. Heterocycl. Chem. 6 1994 36
5. K.C. Joshi, S.K. Jain, and A.K. Jain Curr. Sci. 51 1982 346
6. A.-M.M.E. Omar, N.H. Eshaba, and H.M. Aboushleib J. Heterocycl. Chem. 23 1986 1731
7. B.S. Holla, and K.V. Udupa J. Indian Chem. Soc. 65 1988 524
8. F.F. Abdel-Latif, R.M. Shaker, S.A. Mahgoub, and M.Z.A. Badar J. Heterocycl. Chem. 26 1989 769
9. M.A.E. Shaban, A.Z. Nasr, and A.E. Morgaan A. Farmaco 54 1999 800
10. Kaminsky, D. US Patent 1973, 3, 752-891.
11. A. Monge, J.A. Palop, C. Ramirez, and E. Fernandez-Alvarez Acta Farm Bonaerense 8 1987 157
12. A. Monge, J.A. Palop, C. Ramierz, M. Font, and E. FernandezAlvarez Eur. J. Chem. 26 1991 179
13. A.B. Tomchin, M.A. Ignateva, and G.F. Masyuta KhimFarm Zh 6 1972 23
14. N.H. Eshaba, H.M. Salama, I.M. Labouta, and A.-M.M.E. Omar Pharmazie 42 1987 664
15. M.A.E. Shaban, A.Z. Nasr, and A.E.A. Morgaan Pharmazie 54 1999 580
16. M.A.E. Shaban, M.A.M. Taha, and A.E. Morgaan Monatsh. A. Chem. 131 2000 487
17. V. Ivachtchenko Alexandre, P. Alexey yin' Il, V. Kobak Vladimir, A.Z. Denis, V. Boksha Larisa, S. Andrey Trifilenkov, and M. Ugoleva Dina J. Comb. Chem. 4 2002 419 428
18. R. Sridhar, B. Srinivas, V. Pavan Kumar, V.P. Reddy, A.V. Kumar, and K.R. Rao Adv. Synth. Catal. 350 2008 1489
19. B. Madhav, S.N. Murthy, V.P. Reddy, K.R. Rao, and Y.V.D. Nageswar Tetrahedron Lett. 50 2009 6025
20. S.N. Murthy, B. Madhav, A.V. Kumar, Y.V.D. Nageswar, and K.R. Rao Tetrahedron 65 2009 5251
21. S.N. Murthy, B. Madhav, A.V. Kumar, K.R. Rao, and Y.V.D. Nageswar Helv. Chem. Acta 92 2009 2118
22. J. Shankar, K. Karnakar, B. Srinivas, and Y.V.D. Nageswar Tetrahedron Lett. 51 2010 3938
23. S.N. Murthy, B. Madhav, V. Prakash Reddy, and Y.V.D. Nageswar Tetrahedron Lett. 51 2010 3649
24. K. Ramesh, S.N. Murthy, and Y.V.D. Nageswar Tetrahedron Lett. 52 2011 2362
25. B.S.P. Anil Kumar, B. Madhav, K. Harsha Vardhan Reddy, and Y.V.D. Nageswar Tetrahedron Lett. 52 2011 2862