A green protocol for catalyst-free synthesis of 1-oxo-hexahydroxanthenes in aqueous medium

Comptes Rendus Chimie

Volumn 13, Issue 12, 2010, Pages 1429-1432

  Pore, D M ^a   Shaikh, T S ^a   Undale, K A ^a   Gaikwad, D S ^a  

^a SHIVAJI UNIVERSITY   (India)

Author keywords

Cyclohexane 1,3 dione; Dimedone; Hexahydroxanthene; Octahydroxanthene; Salicylaldehyde; Water

Indexed keywords

EID: 78649877391     PISSN: 16310748     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.crci.2010.06.015     Document Type: Article

References (32)

1. Organic Reactions in Water: Principles, Strategies and Applications, ed. U. M. Lindstrom, Blackwell publishing, Oxford, UK 2007.
2. L. Weber Drug Discov. Today 7 2002 143
3. C. Hulme, and V. Gore Curr. Med. Chem 10 2003 51
4. A. Dömling Chem. Rev 106 2006 17
5. I. Kanizsai, S. Gyäónfalvi, Z. Szadonyi, R. Sillanpää, and F. Fülöp Green Chem 9 2007 357
6. P.T. Anastas, and J.C. Warner Green Chemistry. Theory and Practice 1998 Oxford University Press Oxford, UK
7. P.T. Anastas, and T. Williamson Green Chemistry. Frontiers in benign chemical synthesis and process 1998 Oxford University Press Oxford, UK
8. R.A. Sheldon J. Mol. Catal. A 107 1996 75
9. R. Maggi, F. Bigi, S. Carloni, A. Mazzacani, and G. Sartori Green Chemistry 3 2001 173
10. S. Hatakeyma, N. Ochi, H. Numata, and S. Takano J. Chem. Soc. Chem. Commun 1988 1202
11. G. Song, B. Wang, H. Luo, and L. Yang Catal. Commun 8 2007 673 references cited therein
12. F. Lynen Pure Appl. Chem 14 1967 137
13. E.M.C. Gerard, H. Sahin, A. Encinas, and S. Brase Synlett 17 2008 2702
14. S.M.S.C. Menchen, J.Y.L. Benson, W. Lam, D. Zhen, B.B. Sun, S.H. Rosenblum, M.U.S. Khan, and Taing Chem. Abstr 139 2003 54287f
15. G.A. Reynolds, S.A. Tuccio, and O.G Peterson Chem. Abstr 71 1971 81334c
16. R.C. Hunter, and T. Beveridge J. Appl. Environ. Microbiol 71 2005 2501
17. M. Ahmad, T.A. King, D.K Ko, B.H. Cha, and J. Lee J. Phys. D: Appl. Phys 35 2002 1473
18. W.S. Johnson Angew. Chem. 88 (1976) 33; Angew. Chem., Int. Ed. Engl 15 1976 9
19. R.B. Herbert Nat. Prod. Rep 8 1991 185
20. P. Zhang, Y.D Yu, and Z.H Zhang Synth. Commun 38 24 2008 4474
21. Y.L. Li, H. Chen, Z.S. Zeng, X.S. Wang, D.Q. Shi, and S.J Tu Chin. J. Org. Chem 25 2005 846
22. S. Gowravaram, K. Arundhathi, K. Sudhakar, B.S. Sastry, and J.S. Yadav Synth. Commun 38 20 2008 3439
23. X.S. Wang, D.Q. Shi, Y.L. Li, H. Chen, X.Y. Wei, and Z.M. Zong Synth. Commun 35 2005 97
24. S.J. Barlow, T.W. Bastock, J.H. Clark, and S.R. Cullen Tetrahedron Lett 34 1993 3339
25. T. S. Shaikh, N. G. Patil, S. B. Dongare, U. V. Desai, D. M. Pore, Synth. Commun. 40 (2010) 2215.
26. M.C. Pirrung, and K.D. Sarma Tetrahedron 61 2005 11456
27. H.C. Kolb, M.G. Finn, and K.B. Sharpless Angew. Chem., Int. Ed 40 2001 2004
28. C.-J. Li Chem. Rev 93 1993 2023
29. A. Lubineau Chem. Ind 1996 123
30. F. Fringuelli, O. Piermatti, and F. Pizzo O. Attanasi, D. Spinelli, Targets in Heterocyclic Systems. Italian Society of Chemistry: Rome, l 1997 pp. 57
31. P.A. Organic Synthesis in Water Grieco Blackie Academic and Professional: London 1998
32. A. Meijer, S. Otto, and J.B.F.N. Engberts J. Org. Chem 63 1998 8989 and references cited therein