Green chemistry and modern technology

Theoretical and Experimental Chemistry

Volumn 38, Issue 2, 2002, Pages 69-87

  Pokhodenko, V D ^a   Pavlishchuk, V V ^a  

^a L V PISARZHEVSKII INSTITUTE OF PHYSICAL CHEMISTRY   (Ukraine)

Author keywords

Green chemistry; New chemical processes and activation methods; New chemical technologies

Indexed keywords

EID: 33646653463     PISSN: 00405760     EISSN: 1573935X     Source Type: Journal    
DOI: 10.1023/A:1016080416792     Document Type: Article

References (115)

1. P. T. Anastas and J. C. Wamer, Green Chemistry: Theory and Practice, Oxford Sci. Publ., Oxford (1998).
2. D. L. Hjerensen, D. L. Schutt, and J. M. Boese, J. Chem. Ed., 77, No. 12, 1543 (2000).
3. P. Anastas and R. Lankey, Chem. Brit., No. 5, 26 (2001).
4. P. Tundo, P. Anastas, D. StC. Black, et al., Pure Appl. Chem., 72, No. 7, 1207 (2000).
5. P. Tundo and M. Selva, Chemtech., 25, No. 5, 31 (1995).
6. R. A. Sheldon, Pure Appl. Chem., 72, No. 7, 1233 (2000).
7. V. Elango, M. A. Murphy, B. L. Smith, et al., US Pat. 4981995, Publ. 1991.
8. S. Ratton, Chem. Today, March/April, 3 (1997).
9. A. P. Singh and A. K. Pandey, J. Mol. Catal. A: Chem., 123, No. 2, 127 (1997).
10. A. Corma, Chem. Rev., 95, No. 3, 559 (1995).
11. J. A. Ballantine, J. H. Purnell, and J. M. Thomas, US Pat. 4899319, Publ. 1985.
12. J. A. Ballantine, J. H. Purnell, and J. M. Thomas, European Patent 31252, Publ. 1984.
13. J. Reedijk (ed.), Bioinorganic Catalysis, Marcel Dekker, New York (1993).
14. C. L. Hill (ed.), Activation and Functionalization of Alkanes [Russian translation], Mir, Moscow (1998).
15. S. A. Chavan, D. Srinavas, and P. Ratnasamy, J. Chem. Soc., Chem. Commun., No. 12, 1124 (2001).
16. B. Notari, Stud. Surface Sci. Catal., 37, No. 2, 413 (1988).
17. R. Raja, G. Sankar, and J. M. Thomas, J. Am. Chem. Soc., 123, No. 33, 8153 (2001).
18. J. M. Thomas, R. Raja, G. Sankar, et al., J. Chem. Soc., Chem. Commun., No. 7, 525 (1999).
19. J. M. Thomas, R. Raja, and B. F. G. Johnson, Izv. Akad. Nauk, Ser. Khim., No. 11, 1920 (2001).
20. J. H. Clark, Pure Appl. Chem., 73, No. 1, 103 (2001).
21. M. Misono, I. Ono, G. Koyano, et al., Pure Appl. Chem., 72, No. 7, 1305 (2000).
22. N. Mizuno and M. Misono, Chem. Rev., 98, No. 1, 199 (1998).
23. M. Misono, J. Chem. Soc., Chem. Commun., No. 13, 1141 (2001).
24. K. Sano, H. Uchida, and S. Wakabayashi, Catal. Surv. Jpn., 3, No. 1, 55 (1999).
25. M. G. Hitzler, F. R. Smail, and S. K. Ross, J. Chem. Soc., Chem. Commun., No. 3, 359 (1998).
26. Envirocats-Supported Reagents: Product Information, Contract Chemicals, UK (1994).
27. B. P. Bandgar, L. S. Uppalla, and V. S. Sadavarte, Green Chem., 3, No. 1, 39 (2001).
28. C. Murata, H. Yoshida, and T. Hattori, J. Chem. Soc., Chem. Commun., No. 23, 2412 (2001).
29. J. M. Thomas, R. Raja, G. Sankar, et al., J. Chem. Soc., Chem. Commun., No. 13, 1167 (1999).
30. B. Cornils and E. Wiebus, Rec. Trav. Chim. Pays-Bas, 115, No. 2, 211 (1996).
31. R. Sheldon, J. Chem. Soc., Chem. Commun., No. 23, 2399 (2001).
32. K. R. Seddon, J. Chem. Technol. Biotechnol., 68, No. 2, 347 (1997).
33. C. J. Adams, M. J. Earle, and G. Roberts, J. Chem. Soc., Chem. Commun., No. 20, 2097 (1998).
34. M. J. Earle and K. R. Seddon, Pure Appl. Chem., 72, No. 7, 1391 (2000).
35. C. J. Adams, M. J. Earle, and K. R. Seddon, Green Chem., 2, No. 1, 21 (2000).
36. B. Ellis, W. Keim, and P. Wasserscheid, J. Chem. Soc., Chem. Commun., No. 4, 337 (1999).
37. C. J. Adams, M. J. Earle, and K. R. Seddon, J. Chem. Soc., Chem. Commun., No. 11, 1043 (1999).
38. A. Bösmann, L. Datsevich, A. Jess, et al., J. Chem. Soc., Chem. Commun., No. 23, 2494 (2001).
39. A. Baiker, Chem. Rev., 99, No. 2, 453 (1999).
40. R. Noyori, Chem. Rev., 99, No. 2, 353 (1999).
41. P. G. Jessop, T. Ikariya, and R. Noyori, Chem. Rev., 99, No. 2, 475 (1999).
42. J. L. Kendall, D. A. Canelas, J. Young, et al., Chem. Rev., 99, No. 2, 543 (1999).
43. P. E. Savage, Chem. Rev., 99, No. 2, 603 (1999).
44. O. Kajimoto, Chem. Rev., 99, No. 2, 355 (1999).
45. J. Young and J. M. DeSimone, Pure Appl. Chem., 72, No. 7, 1357 (2000).
46. S. Park and E. F. Gloyona, Fuel, 76, No. 11, 999 (1997).
47. T. Sato, G. Sekiguchi, T. Adschiri, and K. Arai, J. Chem. Soc., Chem. Commun., No. 17, 1566 (2001).
48. K. W. Downey, R. H. Snow, D. A. Hazlrbrck, et al., Innovations in Supercritical Fluids: ACS Symposium Series 608, K. W. Hutchenson and N. R. Foster (eds.), ACS, Washington, DC (1995), p. 313.
49. K. Tanaka and F. Toda, Chem. Rev., 100, No. 3, 1025 (2000).
50. M. Kidwai, Pure Appl. Chem., 73, No. 1, 147 (2001).
51. R. S. Varma, Pure Appl. Chem., 73, No. 1, 193 (2001).
52. G. W. V. Cave, C. L. Raston, and J. L. Scott, J. Chem. Soc., Chem. Commun., No. 21, 2159 (2001).
53. B. F. G. Johnson, S. A. Raynor, D. S. Shephard, et al., J. Chem. Soc., Chem. Commun., No. 13, 1167 (1999).
54. M. Kidwai, P. Misra, and K. R. Bhushan, Polyhedron, 18, No. 18, 2641 (1999).
55. M. Avalos, R. Babiano, J. L. Bravo, et al., Green Chem., 3, No. 1, 26 (2001).
56. M. Csiba, J. Cleophax, A. Loupy, et al., Tetrahedron Lett., 34, No. 11, 1787 (1993).
57. D. Bogdal, J. Pielichowski, and A. Boron, Synlett., 873 (1996).
58. R. S. Varma and R. K Saini, Tetrahedron Lett., 38, No. 12, 4337 (1997).
59. P. de la Cruz, A. de la Hoz, L. M. Font, et al., Tetrahedron Lett., 39, No. 33, 6053 (1998).
60. K. J. Watkins, Chem. Eng. News, 80, No. 6, 17 (2002).
61. R. Varma, Green Chem., 1, No. 2, 43 (1999).
62. V. V. Molchanov and R. V. Buyanov, Usp. Khim., 69, No. 5, 476 (2000).
63. T. F. Grigor'eva, A. P. Barinova, and N. Z. Lyakhov, Usp. Khim., 70, No. 1, 52 (2001).
64. P. McCormick, T. Tsuzuki, J. S. Robinson, and J. Ding, Adv. Mater., 13, No. 12/13, 1008 (2001).
65. W. V. Cave and C. L. Raston, J. Chem. Soc., Chem. Commun., No. 22, 2199 (2000).
66. V. Balzani and L. De Cola (eds.), Supramolecular Chemistry: NATO ASISeries, Kluwer, Dordrecht (1992).
67. J. L. Scott and C. L. Raston, Green Chem., 2, No. 5, 245 (2000).
68. T. Seki, K. Akutsu, and H. Hattori, J. Chem. Soc., Chem. Commun., No. 11, 1000 (2001).
69. K. Rossen, P. J. Pye, L. M. DiMichele, et al., Tetrahedron Lett., 39, No. 1, 6823 (1998).
70. I. Ugi, Pure Appl. Chem., 73, No. 1, 187 (2001).
71. K. Smith, S. Almeer, and C. Peters, J. Chem. Soc., Chem. Commun., No. 24, 2748 (2001).
72. N. Nishiwaki, T. Nagami, T. Kawamura, et al., J. Org. Chem., 64, No. 17, 6476 (1999).
73. P. Dumestre, L. El Kaim, and A. Gregoire, J. Chem. Soc., Chem. Commun., No. 9, 775 (1999).
74. J. H. Chaplin and B. L. Flynn, J. Chem. Soc., Chem. Commun., No. 17, 1594 (2001).
75. R. Furka, Drug Dev. Res., 36, No. 1, 1 (1995).
76. D. MacDowell and J. Nelson, Tetrahedron Lett., 29, No. 3, 385 (1988).
77. S. Heck and P. Dömling, Synlett., 424 (2000).
78. R. W. Armstrong, J. Am. Chem. Soc., 117, No. 32, 7842 (1995).
79. L. Tienze, Chem. Rev., 96, No. 1, 115 (1996).
80. S. E. Denmark and A. Thoransen, Chem. Rev., 96, No. 1, 137 (1996).
81. J. D. Winkler, Chem. Rev., 96, No. 1, 167 (1996).
82. I. Ruy, N. Sonoda, and D. P. Curran, Chem. Rev., 96, No. 1, 177 (1996).
83. E. V. Gorobets, M. S. Miftakhov, and F. A. Valeev, Usp. Khim., 69, No. 12, 1091 (2000).
84. S. E. Denmark and A. Thoransen, J. Org. Chem., 59, No. 24, 5672 (1994).
85. A. Orita, M. Katakami, Y. Yasui, et al., Green Chem., 3, No. 1, 13 (2001).
86. J. Thornton, Pandora's Poison: Chlorine, Health, and New Environmental Strategy, MIT Press, Cambridge (2000).
87. A. Ghosh, S. S. Gupta, and M. J. Bartos, Pure Appl. Chem., 73, No. 1, 113 (2001).
88. W. F. Hoederich and F. Kollmer, Pure Appl. Chem., 72, No. 7, 1273 (2000).
89. W. Aquila, H. Fuchs, O. Wörz, et al., US Pat. 6 013 843, Publ. 2000.
90. R. Taramasso, G. Peregro, and B. Notari, US Pat. 4410501, Publ. 1983.
91. U. Bora, M. K. Chaudhuri, D. Dey, et al., Pure Appl. Chem., 73, No. 1, 93 (2001).
92. A. Stocker, O. Marti, T. Pfammater, et al., German Patent 2 046 556, Publ. 1970.
93. R. J. Linderman, S. Binet, S. R. Petrich, et al., J. Org. Chem., 64, No. 2, 336 (1999).
94. M. Selva, C. A. Marques, and P. Tundo, Gazz. Chim. Ital., 123, No. 9, 515 (1993).
95. Shun-ichi Murahashi, Bull. Chem. Soc. Jpn., 72, No. 11, 2737 (1999).
96. R. S. Varma and R. K. Saini, Tetrahedron Lett. 39, No. 12, 1481 (1998).
97. H. Benhaliliba, A. Derdour, J.-P. Bazureau, et al., Tetrahedron Lett., 39, No. 7, 541 (1998).
98. A. Oussaid and A. Loupy, J. Chem. Res. (S), No. 9, 342 (1997).
99. R. S. Varma and R. Dahiya, Tetrahedron Lett., 38, No. 12, 2043 (1997).
100. C. F. Brooks, H. Ling-Chu, M. McCarron, et al., J. Chem. Soc., Chem. Commun., No. 1, 37 (1999).
101. S. P. Gupte, A. B. Shivarkar, and R. V. Chaudhari, J. Chem. Soc., Chem. Commun., No. 24, 2620 (2001).
102. M. Matthews, Pure Appl. Chem., 73, No. 8, 1305 (2001).
103. J. Li and G. Prentice, J. Electrochem. Soc., 144, No. 12, 4284 (1997).
104. M. A. Cassadei, S. Cesa, F. M. Moracci, et al., J. Org. Chem., 61, No. 2, 380 (1996).
105. M. A. Cassadei, F. M. Moracci, G. Zappia, et al., J. Org. Chem., 62, No. 20, 6754 (1997).
106. V. D. Pokhodenko and V. G. Koshechko, Free Radicals in Biology and Environment: NATO ASI Ser., F. Minisci (ed.), Kluwer Acad. Publ., Netherlands (1997), p. 145.
107. J. M. Wagenknecht, J. Electroanal. Chem., 52, No. 3, 489 (1974).
108. 5 C 07 309/06; Publ. January 15, 1991, Bull. No. 38;
109. Ukrainian Patent No. 791 (1993).
110. P. Calas and A. Commeyras, J. Electroanal. Chem., 89, No. 2, 363 (1978).
111. V. G. Koshechko and V. D. Pokhodenko, Teor. Éksp. Khim., 33, No. 5, 268 (1997).
112. V. G. Koshechko and V. D. Pokhodenko, Izv. Akad. Nauk, Ser. Khim., No. 11, 1843 (2001).
113. M. M. Baizer, Tetrahedron, 40, No. 6, 935 (1984).
114. V. G. Koshechko, V. E. Titov, D. V. Sednev, and V. D. Pokhodenko, "Method for obtaining salts of trifluoromethanesulfonic acid," USSR Inventor's Certificate 1699993, IPC C 07 53/18 C 25 B 3/10, Publ. December 23, 1991, Bull. No. 47.
115. I. I. Moiseev, N. A. Platé, and G. F. Tereshchenko, Izv. Akad. Nauk, Ser. Khim., No 11, 1925 (2001).