Microwave assisted synthesis of 3-(2-chloroquiolin-3-yl)-1-substituted phenyl prop-2-en-1-ones using K2CO3 as a mild, cheap and inexpensive catalyst

International Journal of ChemTech Research

Volumn 2, Issue 2, 2010, Pages

  Tiwari, Vandana ^a   Ali, Parvez ^a   Meshram, Jyotsna ^a  

^a RTM NAGPUR UNIVERSITY   (India)

Author keywords

Chalcones; Claisen Schmidt condensation; Microwave; Solid phase

Indexed keywords

3 (2 CHLOROQUINOLIN 3 YL) 1 (2 BROMOPHENYL) PROP 2 EN 1 ONE; 3 (2 CHLOROQUINOLIN 3 YL) 1 (2,4 DICHOROPHENYL) PROP 2 EN 1 ONE; 3 (2 CHLOROQUINOLIN 3 YL) 1 (3,4 DICHLOROPHENYL) PROP 2 EN 1 ONE; 3 (2 CHLOROQUINOLIN 3 YL) 1 (3,4,5 TRIMETHOXYPHENYL) PROP 2 EN 1 ONE; 3 (2 CHLOROQUINOLIN 3 YL) 1 (4 BROMOPHENYL) PROP 2 EN 1 ONE; 3 (2 CHLOROQUINOLIN 3 YL) 1 (5 BROMO 2 METHOXYPHENYL) PROP 2 EN 1 ONE; 3 (2 CHLOROQUINOLIN 3 YL) 1,4 TOLYL PROP 2 EN 1 ONE; 3 (2 CHLOROQUIOLIN 3 YL) 1 PHENYLPROP 2 EN 1 ONE; 3 (2 CHLOROQUNOLIN 3 YL) 1 O TOLYL PROP 2 EN 1 ONE; 3 (2 CHLROQUINLIN 3 YL) 1 (3 NITROPHENYL) PROP 2 EN 1 ONE; CHALCONE DERIVATIVE; SOLVENT; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; CLAISEN CONDENSATION; HEALTH HAZARD; MICROWAVE IRRADIATION; REACTION ANALYSIS; SOLID PHASE SYNTHESIS; SPECTROSCOPY; STRUCTURE ANALYSIS; SUBSTITUTION REACTION;

EID: 77954693881     PISSN: None     EISSN: 09744290     Source Type: Journal    
DOI: None     Document Type: Article

References (19)

1. Caddick S., Tetrahedron., 1995, 51, 10403.
2. Saini R.K., Choudhary A.S., Joshi Y.C and Joshi P., E-J. Chem., 2005, 2, 9.
3. Nem N.H., Kim Y., You Y.J., Hong D.H., Kim H.M., and Ahn B.Z., Eur.J.Med.Chem., 2003, 38,179.
4. Wu J.H., Wang X.H., Yi Y.H and Lee K.H., Bioorg.Med.Chem.,Lett., 2003, 13, 1813.
5. Wu X., Wilairat P and Go M.L., Bioorg.Med.Chem.Lett., 2002, 12, 2299.
6. Tuchinda P., Reutrakul V., Claison P., Pongprayoon V., Sematong T., Santisuk A.T and Taylor W.C., Phytochem.,2002, 59, 169.
7. Xia Y., Yang Z.Y., Xia P., Bastow K.F., Nakanishi Y., and Lee K.H., Bioorg.Med.Chem.Lett. 2000, 10, 699.
8. Kurth E.F., J.Am.Chem.Soc., 1939, 81, 861.
9. Schrafstatter E and Deutsch S., Chem. Ber., 1948, 81, 489.
10. H. Obera H., Onodera J., Kurihara Y., Bull.Chem.Soc.Japan., 1972, 44, 289.
11. Smith H.E and Paulson M.C., J.Am.Chem.Soc., 1954, 76, 4486.
12. Zurd L and Horowitz R.M., J.Org.Chem., 1961, 26, 2561.
13. Dhar D.N., J.Indian Chem.Soc., 1960, 37, 363.
14. Gilman H and Cason L.F., J.Am.Chem.Soc., 1950, 72, 3469.
15. Guttire J.L and Rabjohn N., J.Org.Chem., 1957, 22, 176.
16. Rochus W and Kickuth R., Chem.Abstr., 1961, 56, 10976.
17. Calloway N.O and Green L.D., J.Am.Chem. Soc., 1937, 59, 809.
18. Kushkov V.K, and Utenkova G.N., Zh.Obs.Khim., 1959, 29, 4038.
19. Kellehar R.G., Mekerkovey M.A., and Vibulgen P., J.Chem.Soc. Chem.Commun. 1980, 486.