Efficient and mild room temperature reduction of benzophenones under ultrasound irradiation

Ultrasonics Sonochemistry

Volumn 12, Issue 3, 2005, Pages 169-172

  Peng, Yanqing ^a   Zhong, Wujun ^a   Song, Gonghua ^a  

^a EAST CHINA UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

Benzhydrols; Benzophenones; Reduction; Ultrasound; Zinc

Indexed keywords

BENZENE; ETHANOL; PHENOLS; REDUCTION; SODIUM COMPOUNDS; SYNTHESIS (CHEMICAL);

ROOM TEMPERATURE; ULTRASOUND IRRADIATION;

SONOCHEMISTRY;

BENZOPHENONE DERIVATIVE; PHTHALIDE DERIVATIVE; SODIUM HYDROXIDE; ZINC;

ARTICLE; CHEMICAL MODIFICATION; ELECTRON; IRRADIATION; PRIORITY JOURNAL; REDUCTION; ROOM TEMPERATURE; ULTRASOUND;

EID: 5644294672     PISSN: 13504177     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ultsonch.2003.12.002     Document Type: Article

References (44)

1. Yung D.K., Gilroy M.L., Mahony D.E. J. Pharm. Sci. 67:1978;900
2. Abraham D.J., Kennedy P.E., Mehanna A.S., Patwa D.C., Williams F.L. J. Med. Chem. 27:1984;967
3. Meltzer P.C., Liang A.Y., Madras B.K. J. Med. Chem. 39:1996;371
4. Fischer E., Fischer O. Justus Liebigs Ann. Chem. 194:1878;290
5. Cohen R. Recl. Trav. Chim. Pays-Bas. 38:1919;121
6. Gopalakrishnan G., Babu M.E.P., Pai B.R. Indian J. Chem. Sect. A. 20:1981;998
7. Gunasekaran S., Venkatasubramanian N. J. Chem. Soc., Perkin Trans. 2. 1983;949
8. Nishida S. J. Org. Chem. 32:1967;2692
9. Mindl J., Vecera M. Collect. Czech. Chem. Commun. 37:1972;1143
10. Pavia M.R., Lobbestael S.J., Nugiel D., Mayhugh D.R., Gregor V.E., Taylor C.P., Schwarz R.D., Brahce L., Vartanian M.G. J. Med. Chem. 35:1992;4238
11. Yamataka H., Miyano N., Hanafusa T. J. Org. Chem. 56:1991;2573
12. Lee D.G., Raptis M. Tetrahedron. 29:1973;1481
13. Zeiss T. J. Am. Chem. Soc. 75:1953;897
14. Yamataka H., Miyano N., Hanafusa T. J. Org. Chem. 56:1991;2573
15. Muraoka M., Itoh T., Mizuma T., Toyoshima S. Chem. Pharm. Bull. 8:1960;860
16. Bachmann C., Carlson E. Jr., Moran J.C. J. Org. Chem. 13:1948;916
17. Hattori K., Sajiki H., Hirota K. Tetrahedron. 57:2001;4817
18. Sajiki H., Hattori K., Hirota K. J. Chem. Soc., Perkin Trans. 1. 1998;4043
19. Ohkuma T., Koizumi M., Ikehira H., Yokozawa T., Noyori R. Org. Lett. 2:2000;659
20. Sopher D.W., Utley J.H.P. J. Chem. Soc., Perkin Trans. 2. 1984;1361
21. Sivakumar A., Jayarama Reddy S., Krishnan V.R. Indian J. Chem. Sect. A. 22:1983;800
22. Norris J.F., Blake J.T. J. Am. Chem. Soc. 50:1928;1808
23. Hughes E.D., Ingold C.K., Taher N.A. J. Chem. Soc. 1940;949
24. Lorimer J.P., Mason T.J. Chem. Soc. Rev. 16:1987;239
25. Lindley J., Mason T.J. Chem. Soc. Rev. 16:1987;275
26. Suslick K.S. Sci. Am. 260:1989;80
27. Einhorn C., Einhorn J., Luche J. Synthesis. 1989;787
28. Hunicke R.L. Ultrasonics. 28:1990;291
29. Berlan J., Mason T.J. Ultrasonics. 30:1992;203
30. Mason T.J. Chem. Soc. Rev. 26:1997;443
31. Cintas P., Luche J. Green Chem. 1:1999;115
32. Sato R., Nagaoka T., Goto T., Saito M. Bull. Chem. Soc. Jpn. 63:1990;290
33. Zhong W., Song G., Peng Y., Qian X. Synth. Commun. 30:2000;3801
34. Peng Y., Song G. Green Chem. 3:2001;302
35. Peng Y., Song G. Green Chem. 4:2002;349
36. Yokoe I., Higuchi K., Shirataki Y., Komatsu M. Chem. Pharm. Bull. 29:1981;894
37. Truett W.L. J. Am. Chem. Soc. 73:1951;5913
38. Isola M., Ciuffarin E., Sagramora L. Synthesis. 1976;326
39. Streitwieser A. Jr., Vorpagel E.R., Chen C.-C. J. Am. Chem. Soc. 107:1985;6970
40. Trahanovsky W.S., Lawson J.A., Zabel D.E. J. Org. Chem. 32:1967;2287
41. Bokadia M.M., Brown B.R., Cummings W. J. Chem. Soc. 1960;3308
42. Tobia D., Rickborn B. J. Org. Chem. 51:1986;3849
43. Zagumenny A. Chem. Ber. 14:1881;1402
44. Gomberg M., Bachmann W.E. J. Am. Chem. Soc. 49:1927;236