An efficient use of zeolite catalysts for esterification of carboxylic acids

Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry

Volumn 35, Issue 11, 1996, Pages 1174-1179

  Gumaste, Vikas K ^a   Deshmukh, A R A S ^a   Bhawal, B M ^a  

^a NATIONAL CHEMICAL LABORATORY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0041334074     PISSN: 03764699     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (41)

1. Oblad A G, Oil Gas J, 70, 1972, 84.
2. (a) Benesi H A, J Catal, 7, 1967, 386.
3. (b) Vento P B, Hamilton L A, Landis P S & Wise J J, J Catal, 5, 1966, 81.
4. (c) Daage M & Fajula F, Bull Soc Chem Fr, 5, 1984, 153 & 163.
5. (d) Hoelderich W F, In: Heterogeneous catalysis and fine chemicals, edited by M Guisnet et al. (Elsvier Science Publishers, B V, Amsterdam) 1988, p83.
6. (a) Breck D W, J Chem Edn, 41, 1964, 678.
7. (b) Breck D W, Zeolite molecular Sieves. (John Wiley and Sons, New York) 1974.
8. (c) Rabo J A, Zeolite chemistry and catalysts, ACS Monograph 171 (American Chemical Society, Washington DC) 1976.
9. (a) Deshmukh ARAS, Reddy T I, Bhawal B M, Shiralkar V P & Rajappa S, J Chem Soc, Perkin Trans-1, 1990, 1217.
10. (b) Reddy T I, Bhawal B M & Rajappa S, Tetrahedron Lett, 33, 1992, 2857.
11. (c) Reddy T I, Bhawal B M & Rajappa S, Tetrahedron, 49, 1993, 2101.
12. (d) Bhawal B M, Vetrivel R, Reddy T I, Deshmukh A R A S & Rajappa S, J Phys Org Chem, 7, 1994, 377.
13. (e) Bhawal B M, Mayabhate S P, Likhite A P & Deshmukh A R A S, Synth Commun, 25, 1995, 3315.
14. (f) Deshmukh A R A S, Gumaste V K & Bhawal B M, Synth Commun, 25, 1995, 3939.
15. (a) Davis M E, Acc Chem Res, 26, 1993, 111.
16. (b) Holderich W F, Hesse M & Naumanns F, Angew Chem Int Ed Engl, 27, 1988, 226.
17. (c) Suib S L, Chem Rev, 93, 1993, 803.
18. (d) Sachtler W M H, Acc Chem Res, 26, 1993, 383.
19. Haslam E, Tetrahedron, 36, 1980, 2409 and references cited therein.
20. Khurana J M, Sahoo P K & Maikap G C, Synth Commun, 20, 1990, 2267 and references cited therein.
21. Holderich W F, Hesse M & Naumann F, Angew Chem Int Ed Engl, 27, 1988, 226 and references cited therein.
22. Gregory R & Westlake D J, Eur Patent EP 45618, 1982; Chem Abstr, 96, 1982, 149899q.
23. Ronghu H, Qingzhi C & Zheng Y, Faming Zhuanli Shenqing Gongkai Shuomingshu C N, 85, 102395, 1986; Chem Abstr, 108, 1988, 133817s.
24. Dusan M, Jan V, Milina C & Jan I, Czech CS 256,085, 1988; Chem Abstr, 111, 1989, 96846q.
25. Knifton J F, US Patent US 5,081,318, 1992; Chem Abstr, 116, 1992, 105622w.
26. Dafu M, Huazue Shiji, 30, 1989, 247; Chem Abstr, 112, 1990, 58678z.
27. Dafu M, Huazue Shiji, 30, 1989, 247; Chem Abstr, 112, 1990, 58678z.
28. Zhenhua Z, & Wang Y , Human, Shifen Daxue Kexue Xuebao, 13, 1990, 61; Chem Abstr, 114, 1991, 2606.
29. Zhenhua Z, & Wang Y , Human, Shifen Daxue Kexue Xuebao, 13, 1990, 61; Chem Abstr, 114, 1991, 2606.
30. Vogel A I, Practical organic chemistiy, 4th Edn (ELBS), 1987, pp 501-515.
31. Shaw R & Elliot W H, J Lipid Res, 19, 1978, 783.
32. Ballini R & Carotti A, Synth Commun, 13, 1983, 1197.
33. Neises B & Stelich W, Angew Chem Int Ed Engl, 17, 1978, 522.
34. Shiralkar V P & Kulkarni S B, Indian J Chem. 16A, 1978, 665.
35. Handbook of chemistry and physics, 61 st Edn, edited by R C West (CRC Press Inc: Cleveland, Ohio) 1980-1981.
36. Rajyam B S, Haranadh C & Murty C R K, Indian J Pure Appl Phys, 6, 1968, 16.
37. Hodgkinson W R, J Chem Soc, 27, 1880, 483.
38. Laato H, Isotalo R, Acta Chem Scand, 21, 1967, 2119.
39. Eremyan E V & Davtyan K A, Prom-st Arm (USSR). 1977, 43; Chem Abstr, 88, 1978, 78159v.
40. Eremyan E V & Davtyan K A, Prom-st Arm (USSR). 1977, 43; Chem Abstr, 88, 1978, 78159v.
41. Perkin W H, J Chem Soc, 69, 1896, 1471.