β-Cyclodextrin mediated MCR in water: Synthesis of dihydroisoindolo[2,1-a]quinazoline-5,11-dione derivatives under microwave irradiation

Tetrahedron Letters

Volumn 54, Issue 49, 2013, Pages 6744-6746

  Reddy, G Rajeshwar ^a,b   Reddy, T Ram ^a   Chary, R Gangadhara ^a   Joseph, Suju C ^a   Mukherjee, Soumita ^c   Pal, Manojit ^c  

^a DR REDDY'S LABORATORIES LTD   (India)

^b JAWAHARLAL NEHRU TECHNOLOGICAL UNIVERSITY   (India)

^c INSTITUTE OF LIFE SCIENCES   (India)

Author keywords

CD; Dihydroisoindolo 2,1 a quinazoline 5,11 dione; MCR; Microwave; Water

Indexed keywords

BETA CYCLODEXTRIN; DIHYDROISOINDOLO[2,1 ALPHA ]QUINAZOLINE 5,11 DIONE DERIVATIVE; QUINAZOLINE DERIVATIVE; UNCLASSIFIED DRUG; WATER;

ARTICLE; CATALYST; CHEMICAL REACTION; COMBINATORIAL LIBRARY; HEATING; MICROWAVE IRRADIATION; REACTION TIME; SYNTHESIS;

EID: 84886947759     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2013.09.138     Document Type: Article

References (20)

1. For recent in depth reviews, see: B.B. Toure, and D.G. Hall Chem. Rev. 109 2009 4439
2. B. Ganem Acc. Chem. Res. 42 2009 463
3. For a thematic series, see: 'Multicomponent reactions' T.J.J. Müller Beilstein J. Org. Chem. 7 2011 950 1507
4. A. Kumar, V.D. Tripathi, and P. Kumar Green Chem. 13 2011 51
5. S.N. Murthy, B. Madhav, A.V. Kumar, K.R. Rao, and Y.V.D. Nageswar Helv. Chim. Acta 92 2009 2118
6. K. Pfeffer Cytokine Growth Factor Rev. 14 2003 185
7. N. Scheinfeld J. Dermatolog. Treat. 15 2004 280
8. D. Shiu-Hin Chan, H.-M. Lee, F. Yang, C.-M. Che, C.C.L. Wong, R. Abagyan, C.-H. Leung, and D.-L. Ma Angew. Chem.; Int. Ed. 49 2010 2860
9. For our earlier endeavour on the synthesis of bioactive novel small molecules, see: K.S. Kumar, P.M. Kumar, M.A. Reddy, M. Ferozuddin, M. Sreenivasulu, A.A. Jafar, G.R. Krishna, C.M. Reddy, D. Rambabu, K.S. Kumar, S. Pal, and M. Pal Chem. Commun. 2011 10263
10. G.R. Reddy, T.R. Reddy, S.C. Joseph, K.S. Reddy, L.S. Reddy, P.M. Kumar, G.R. Krishna, C.M. Reddy, D. Rambabu, R. Kapavarapu, C. Lakshmi, T. Meda, K.K. Priya, K.V.L. Parsa, and M. Pal Chem. Commun. 2011 7779
11. P.M. Kumar, K.S. Kumar, P.K. Mohakhud, K. Mukkanti, R. Kapavarapu, K.V.L. Parsa, and M. Pal Chem. Commun. 2012 431
12. B. Prasad, R. Adepu, S. Sandra, D. Rambabu, G.R. Krishna, C.M. Reddy, G.S. Deora, P. Misra, and M. Pal Chem. Commun. 2012 10434
13. R. Adepu, R. Sunke, C.L.T. Meda, D. Rambabu, G.R. Krishna, C.M. Reddy, G.S. Deora, K.V.L. Parsa, and M. Pal Chem. Commun. 2013 190
14. K.S. Kumar, P.M. Kumar, K.A. Kumar, M. Sreenivasulu, A.A. Jafar, D. Rambabu, G.R. Krishna, C.M. Reddy, R. Kapavarapu, K.S. Kumar, K.K. Priya, K.V.L. Parsa, and M. Pal Chem. Commun. 2011 5010
15. C.J. Li Chem. Rev. 93 1993 2023
16. C.O. Kappe, and D. Dallinger Nat. Rev. Drug Disc. 5 2006 51
17. V. Polshettiwar, and R.S. Varma Acc. Chem. Res. 41 2008 629
18. V. Polshettiwar, and R.S. Varma Chem. Soc. Rev. 37 2008 1546
19. S.A. Galema, B.S.J. Halstead, and D.M.P. Mingos Chem. Soc. Rev. 2 1998 213
20. R. Trotzki, M. Nuchter, and B. Ondruschka Green Chem. 5 2003 285