Hydrated ferric perchlorate, Fe(ClO4)3.XH 2O in organic synthesis. A short review

Journal of the Iranian Chemical Society

Volumn 4, Issue 4, 2007, Pages 375-392

  Heravi, M M ^a   Behbahani, F K ^a  

^a ALZAHRA UNIVERSITY   (Iran)

Author keywords

Carbon carbon cleavage and formation; Catalyst; Ferric perchlorate; Multi component reaction; Oxidation

Indexed keywords

EID: 36549080145     PISSN: 1735207X     EISSN: 17352428     Source Type: Journal    
DOI: 10.1007/BF03247223     Document Type: Article

References (259)

1. a) H. Yamamoto, Lewis Acids in Organic Synthesis, Wiley-VCH, 2 (2001) 597;
2. b) R.A. Sheldon, R.S. Downing, Appl. Catal. A. Gen. 189 (1999) 163;
3. c) R.S. Varma, Green Chem. 1 (1999) 43.
4. B. Kumar, H. Kumar, M. Singh, Indian J. Chem. 30B (1991) 460.
5. B. Kumar, H. Kumar, B. Kaur, Indian J. Chem. 30B (1991) 869.
6. B. Kumar, H. Kumar, A. Parmar Synth. Commun. 22 (1992) 1087.
7. B. Kumar, H. Kumar, A. Parmar Indian J. Chem. 32B (1993) 292.
8. A. Citterio, R. Sebastiano, M.C. Carvayal, J. Org. Chem. 56 (1991) 5335.
9. E. Kotani, S. Kobayashi, Y. Ishii, S. Tobinaga, Chem. Pharm. Bull. 32 (1984) 4281.
10. R.A. Home, Phys. Chem. 62 (1958) 509.
11. P. Salehi, A. Rostamian Motiagh, Synth. Commun. 30 (2000) 671.
12. W.N. White, B.E. Norcross, J. Am. Chem. Soc. 83 (1961) 3265.
13. E.M. Marks, D. Lipkin, B. Bettman, J. Am. Chem. Soc. 59 (1937) 946.
14. W.T. Olson, H.F. Hipsher, C.M. Buess, I.A. Goodman, I. Hart, J.R. Lamneck, L.C. Gibbons, J. Am. Chem. Soc. 69 (1947) 2451.
15. R.A. Dubios, Diss. Abstr. Bit. B. 37 (1976) 223.
16. S.R. Sandier, Organic Functional Group Preparation, Academic Press, 1 (1986) 139.
17. B.H. Shoemaker, C.E. Boord, J. Am. Chem. Soc. 53 (1931) 1505.
18. S. Torii, S. Takagishi, T. Inokuchi, H. Okumoto, Bull. Chem. Soc. Jpn. 60 (1987) 775.
19. C.D. Nenitzescu, V. Przemetzki, Chem. Ber. 69B (1936) 2706.
20. H.C. Chitwood, B.T. Freure, J. Am. Chem. Soc. 68 (1964) 680.
21. Y. Kashman, J. Org. Chem. 37 (1972) 912.
22. N. Iranpoor, E. Mothaghineghad, Tetrahedron 50 (1994) 1859.
23. N. Iranpoor, E. Mothaghineghad, Synth. Commun. 25 (1995) 2253.
24. P. Salehi, N. Iranpoor, F.K. Behbahani, Tetrahedron 54 (1998) 943.
25. N. Iranpoor, E. Mothaghineghad, Tetrahedron 50 (1994) 7299.
26. E.F. Pratt, J.D. Draper, J. Am. Chem. Soc. 71 (1949) 2846.
27. J.A. Zoltewiez, A.A. Sale, J. Org. Chem. 35 (1970) 3462.
28. W.H. Watanabe, L.E. Conlon, J. Am. Chem. Soc. 79 (1957) 2828.
29. P. Salehi, B. Seddighi, M. Irandoost, F.K. Behbahani, D.P. Tahmasbi, Synth. Commun. 30 (2000) 1743.
30. rd ed, Jhon Wiley & Sons. New York, 1999, p. 150.
31. Aromatic Chemicals, Perfumes and Flavour Technology, Sbp Board of Consultants and Engineers, Sbp Chemical Engineers Series No. 54 (Small Business Publications Delhi).
32. E. Haslam, Tetrahedron 36 (1980) 2409.
33. J. Aracil, M. Martinez, N. Sanchez, A. Corma, Zeolites 12 (1992) 233.
34. F.F. Bamoharram, M.M. Heravi, M. Roshani, A.G. Jahangir, Applied Catalysis A: General 302 (2006) 42.
35. J.S. Yadav, B.V.S. Reddy, A.D. Krishna, Ch. Suresh Reddy, A.V. Narsaiah, J. Mol. Catal. A: Chemical 261 (2007) 93.
36. B. Kumar, A. Parmar H. Kumar, Indian J. Chem. B-Organic Chemistry Including Medicinal Chemistry 33 (1994) 698.
37. B. Kumar, H. Kumar, A. Parmar, Indian J. Chem. B-Organic Chemistry Including Medicinal Chemistry 32 (1993) 292.
38. a) A. Parmar, J. Kaur, R. Goyal, B. Kumar, H. Kumar, Synth. Commun. 28 (1998) 2821;
39. b) A. Parmar, R. Goyal, B. Kumar, H. Kumar, Synth. Commun. 29 (1999) 139.
40. P. Salehi, M.M. Khodaei, S.B. Ghareghani, A.R.
41. Motlagh, Russ. J. Org. Chem. 39 (2003) 794.
42. A.L. Pearson, W.J. Handbook Or Reagents For Organic Synthesis, Acetylating Agents and Protecting Groups, John Wiley & Sons, UK, 1999, pp. 9-16.
43. S. Chandrasekhar, T. Roma Chander, M. Takhi, Tetrahedron Lett 39 (1998) 3263.
44. R. Dalpazzo, A. De Nino, L. Maiuolo , A. Procopio, M. Nardi, G. Bartali, R. Romeo, Tetrahedron Lett. 44 (2003) 5621.
45. M. Moghadam, S. Tangestaninejad, V. Mirkhani, I. Mohammadpour Baltrork, R. Shabani, J. Mol. Catal. A: Chemical 219 (2004) 73.
46. S. Gowda, K.M. Lokanatha Rai, J. Mol. Catal. A: Chemical 217 (2004) 27.
47. S.G. Lee, J.H. Park, J. Mol. Catal. A: Chemical 194 (2003) 49.
48. R. Ballini, G. Bosica, S. Carloni, L.Ciaralli, R. Maggi, G. Sortori, Tetrahedron Lett. 39 (1998) 6049.
49. P.A. Procopiou, S.P.D. Baugh, S.S. Flack, G.G.A. Inglis, J. Org. Chem. 63 (1998) 2342.
50. P. Saravanan, V.K. Singh, Tetrahedron Lett. 40 (1999) 2611.
51. E .Vedejs, O. Dougulis, J. Org. Chem. 61 (1996) 5702.
52. K. Ishehara, M. Kulata, H. Karihara, H. Yamamato, J. Am. Chem. Soc. 117 (1995) 4413.
53. K.K. Chauhan, C.G. Frost, I. Love, D. Wait, Synlett (1999) 1743.
54. M.D. Carrigan, R.S. Mohan, Synthesis 14 (2001) 2091.
55. B.M. Choudary, M. Lakshmi, M. Kantan, V. Neeraja, T. Bandyopadhyay, P. Nassi. Reddy, J. Mol. Catal. A: Chemical 140 (1999) 25.
56. P. Phukan, Tetrahedron Lett. 45 (2004) 4785.
57. Y. Nakae, I. Kusati, T. Sato, Synlett 10 (2001) 1584.
58. G. Bartoli, M. Bosco, R. Dalpozzo, E. Marcantoni, M. Massaccesi, S. Rinaldi, L. Sambri, Synlett (2003) 39.
59. G. Bartoli, M. Bosco, R. Dalpozzo, E. Marcantoni, E. Massaccesi, L. Sambri, Eur. J. Org. Chem. (2003) 4611.
60. J. Otera, Angew. Chem. Int. Ed. 1 (2001) 2044.
61. M.M. Heravi, F.K. Behbahani, F.F. Bamoharram, J. Mol. Catal. A: Chemical 253 (2006) 16.
62. M.M. Heravi, F.K. Behbahani, R. Hekmat Shoar, H.A. Oskooie, Cat. Commun.7 (2006) 136.[59] A. Khan, S. Islam, L.H. Choudhurg, S. Ghosh,
63. Tetrahedron Lett. 45 (2004) 9617.
64. Y.-G. Wang, X.-X. Wu, Z.-Y. Jiang, Tetrahedron Lett. 45 (2004) 2973.
65. T. Ikawa, H. Sajiki, K. Hirota, Tetrahedron Lett. 60 (2004) 6189.
66. I.E. Marko, A. Ates, B. Augustyns, A. Gautier, Y. Quesnel, L. Turet, M. Wiaux, Tetrahedron Lett. 40 (1999) 5613.
67. B. Ganem, J.R.V.R. Small, J. Org. Chem. 39 (1974) 3728.
68. M. Schwartz, R.M. Waters, Synthesis (1972) 567.
69. S. Chandrasekhar, T. Ramachander, M.V. Reddy, M. Takhi, J. Org. Chem. 65 (2000) 4729.
70. I. Mohammad Poor Baltork, A.R. Khosropour, Monatsch. Chem. 133 (2002) 189.
71. K.L. Chandra, O. Saravanan, V.K. Singh, Tetrahedron Lett. 42 (2001) 5309.
72. C.S. Reddy, G. Smith, S. Chandrasekhar, Tetrahedron Lett. 44 (2003) 4693.
73. M.M. Heravi, F.K. Behbahani, R. Hekmat Shoar, H.A. Oskooie, J. Mol. Catal. A: Chemical 244 (2006) 8.
74. T. Kino, H. Hatanaka, M. Hasshimoto, M. Nishisyma, T. Goto, M. Okuhara, M. Kohsaka, H. Aoki, H. Imanaka, J. Antibiot. 40 (1987) 1249.
75. a) G.H. Posner, D.Z. Rogers, J. Am. Chem. Soc. 99 (1977) 8208;
76. b) G.A. Olah, A.P. Fung, D. Meidar, Synthesis (1981) 280;
77. c) C. Moberg, L. Rakos, L. Tome, Tetrahedron Lett. 3 (1992) 2191;
78. d) N. Iranpoor, P. Salehi, Synthesis (1994) 1152;
79. e) P. Stead, H. Marley, M. Mahmoudian, G. Webb, D. Noble, Y.T. Ip, E. Piga, T. Rossi, S. Roberts, M.J. Dawson, Tetrahedron Asymmerty 7 (1997) 2247;
80. f) J. Xin, J. Suo, X. Zhang, Z. Zhang, New J. Chem. 24 (2000) 569;
81. g) C.J. Salomon, Synlett (2001) 65;
82. h) C. Jaramillo, J.L. Chiara, M. Martin-Lomas, J. Org. Chem. 59 (1994) 3135;
83. i) C. Moberg, L. Rakos, L. Tottie, Tetrahedron Lett. 33 (1992) 2191;
84. j) N. Iranpoor, T. Tarrian, Z. Movahedi, Synthesis (1996) 1473;
85. k) N. Iranpoor, H. Adibi, Bull. Chem. Soc. Jpn. 73 (2000) 675;
86. l) B.M. Choudary, Y. Sudha, Synth. Commun. 26 (1996) 2989;
87. m) N. Iranpoor, M. Shekarriz, F. Shiriny, Synth. Commun. 28 (1998), 347;
88. n) N. Iranpoor, I. Mohammadpoor Baltork, F. Shirini, Tetrahedron 47 (1991) 9861;
89. o) B. Tamami, N. Iranpoor, M.A. Karimi Zarchi, Polymer 34 (1993) 2011;
90. p) V. Mirkhani, S. Tangestaninejad, B. Yadollahi, L. Alipanah, Tetrahedron 59 (2003) 8213;
91. q) M.L. Kantam, K. Aziz, K. Jeyalakshmi, P.R. Likhar, Catal. Lett. 89 (2003) 95;
92. r) P. Salehi, B. Seddighi, M. Irandoost, F.K. Behbahani, Synth. Commun. 30 (2000) 2967.
93. P. Salehi, B. Seddighi, M. Irandoost, F.K. Behbahani, Synth. Commun. 30 (2000) 2967.
94. a) T. Neshiguchi, K. Karamine, J. Chem. Soc., Chem. Commun. (1990) 1776;
95. b) T. Neshiguchi, S. Fuyrsahi, M. Kurodo, K. Kayesaki, M. Saiteh, J. Org. Chem. 63 (1998) 8183;
96. c) S. Chandrasekhar, M. Takhi, R. Reddy, S. Maharatra, Tetrahedron 57 (2001) 4405;
97. d) N. Deka, J.C Sarma, J. Org. Chem. 66 (2001) 1947;
98. e) N. Deka, J.C. Sarma, Synth. Commun. 30 (2000) 4435, and References Cited Therein;
99. f) B.C. Ranu, M. Saha, J. Org. Chem. 59 (1994) 826;
100. g) J.N. Canydo, A. Garcia, F. Lafont, D. Luna, J.M. Marenas, Synth. Commun. 24 (1994) 1345;
101. h) S. Nak, R. Gaymath, B.K. Patel, Tetrahedron Lett. 42 (2001) 7679;
102. i) A. Manar, T. Beregszaszi, Tetrahedron Lett. 37 (1996) 8597;
103. L.C. Branco, C.A.M. Afonso, Tetrahedron 57 (2001) 4405;
104. j) B.S. Babu, K.K. Balasubramanian, Tetrahedron Lett. 39 (1998) 9287;
105. k) M.M. Heravi, F.K. Behbahani, R.H. Shoar, H.A. Oskooie, J. Mol. Catal. A-Chemical 244 (2006) 8;
106. l) M.M. Heravi, P. Kazemian, H.A. Oskooie, M. Ghassemzadeh, J. Chem. Res. (S) (2005) 105;
107. m) M.M. Heravi, F.K. Behbahani, H.A. Oskooie, R.H. Shoar. Tetrahedron Lett. 46 (2005) 2543;
108. n) M.M. Heravi, H.A. Oskooie, L. Sangsefidi. M. Ghassemzadeh, K. Tabarhydar Phosphorus Sulfur And Silicon and the Related Elements 177 (2002) 2843;
109. o) B. Mohajerani, M.M. Heravi, D. Ajami, Monatshefte Fur Chemie 132 (2001) 871;
110. p) M.M. Heravi, D. Ajami, M. Ghassemzadeh Synthesis (1999) 393;
111. q) M.M. Heravi, M. Haghighi, F. Derikvand, F.F. Bamoharram, Synth. Commun. 36 (2006) 3103.
112. a) S. Hoyer, P. Laszlo, M. Orlonic, E. Pallo, Synthesis (1986) 65;
113. b) B.P. Bandgaz, S.R. Jagtap, B. Aghade, P. Wadgaonkar, C.U. Deresh, R.S. Reddy, B. Pandey, Synthesis (1993) 1069;
114. c) R. Balline, F. Bigi, S. Carloni, R. Maggi, G. Sartoni, Tetrahedron Lett. 38 (1997) 4169;
115. d) I. Rodriguez, M.J. Clemant, S. Ilona, V. Fornes, A. Corma, J. Catal. 192 (2000) 44;
116. e) K.R. Kleetstra, H. Vanbekkum, J. Chem. Res. (S) (1995) 26;
117. f) M.M. Heravi, D. Ajami, M. Ghassemzadeh, Synth. Commun. 29 (1999) 1013;
118. g) S. Chandrasekhar, M. Takhi, Y.R. Reddy, S. Maharatra, C. Rao, K.V. Reddy, Tetrahedron 53 (1997) 14997;
119. h) A.S. Garare, D.P. Salde, M.S. Shengare, R.D. Wakharkar, Synth. Commun. 32 (2002) 1549.
120. Y.S. Han, C.C. Lee, R.J. Chen, P.H. Szu, Tetrahedron 57 (2001) 5991.
121. a) M. Miyashita, A. Yoshikoshi, P. Grieco, J. Org. Chem. 42 (1977) 3772;
122. b) E.J. Corey, H. Niwa, J. Knolle, J. Am. Chem. Soc. 100 (1978) 1942;
123. c) K. Bernardy, M.B. Floyd, J.F. Poletto, M.J. Weiss, J. Org. Chem. 44 (1979) 1438;
124. d) Y. Ogawa, M. Shibasaki, Tetrahedron Lett. 25 (1984) 663;
125. e) A. Fadei, J. Salaun, Tetrahedron 41 (1985) 1267;
126. f) D. Gala, M. Steinman, R.S. Jaret, J. Org. Chem. 51 (1986) 4488;
127. g) S. Kim, J.H. Park, Tetrahedron Lett. 23 (1987) 393;
128. h) K.P. Nambiar, A. Mitra, Tetrahedron Lett. 35 (1994) 3033;
129. i) K. Zimmermann, Synth. Commun. 25 (1995) 2959;
130. j) A.S.-Y. Lee, F.-Y. Su, Y.-C. Liao, Tetrahedron Lett. 40 (1999) 1323;
131. k) G.P. Ramanelli, C. Baronetti, H.J. Thomas, J.C. Autino, Tetrahedron Lett. 43 (2002) 7589;
132. l) M.H. Habibi, S. Tangestaninejad, I. Mohammadpoor-Baltrok, V. Mirkhani, B. Yadollahi, Tetrahedron Lett. 57 (2001) 2851;
133. m) M.M. Heravi, D. Ajami, M. Ghassemzadeh, Synth. Commun. 29 (1999) 1013.
134. M.M. Heravi, F.K. Behbahani, H.A. Oskooie, R. Hekmat Shoar, Tetrahedron Lett. 46 (2005) 2543.
135. J. J. Gregory, J. Chem. Soc. B (1970) 1201.
136. a) B.B. Sinder, S.G. Amin, Synth. Commun. (1978) 117;
137. b) I. Freeman, E.M. Karchetski, J. Chem. Eng. Data. 22 (1977) 335.
138. E.J. Knoevenagel, Liebigs Ann. Chem. 402 (1905) 111.
139. P. Claussner, Ber. Dtsch. Chem. Ges. 38 (1905) 2860.
140. H. Firouzababi, N. Iranpoor, F. Nowrouz, K. Amani, Tetrahedron Lett. 44 (2003) 3951.
141. R. Ghosh, S. Maiti, A. Chakraborty, R. Halder, J. Mol. Catal. A: Chemical 215 (2004) 49.
142. D.H. Aggen, J.N. Arnold, P.D. Hayes, N.J. Smoter, R.S. Mohan, Tetrahedron 60 (2004) 3675.
143. N. Ziyaei, N. Azizi, M.R. Saidi, J. Mol. Cat. A: Chemical 238 (2005) 138.
144. M.M. Heravi, F.K. Behbahani, R. Hekmat Shoar, H.A. Oskooie, Mendeleev Commun, submitted.
145. J.J. Ritter, P.P. Minieri, J. Am. Chem. Soc. 70 (948) 4045.
146. a) J.A. Sanguigni, R. Levins, J. Med. Chem. 7 (1964) 573;
147. b) F. Alonso Cermono, R.M. Obeso Caceres, Anal. Quim. 74 (1978) 778.
148. A. Carcia Martinez, R. Martinez Alvarez, E. Teso Vilar, A. Garcia Fraile, M. Hanach, L.R. Subramanian, Tetrahedron Lett. 30 (1989) 581.
149. a) D.H.R. Barton, P.D. Magnus, R.N. Young, J. Chem. Soc. Chem. Commun. (1973) 331;
150. b) D.H. R. Barton, P.D. Magnus, J.A. Garbarino, R.N. Young, J. Chem. Soc. Perkin Trans. 1 (1974) 2101.
151. H. Firouzabadi, A.R. Sardarian, H. Badparva, Synth. Commun. 24 (1994) 601.
152. G.A. Olah, T. Yamato, S. Lyer, Mater. Chem. Phys. 17 (1987) 21.
153. M. Mukhopadhyay, M.M. Reddy, G.C. Maikap, J. Iqbal, J.Org. Chem. 60 (1995) 2670.
154. M. Mukhopadhyay, J. Iqbal, J. Org. Chem. 62 (1997) 1843.
155. A. Parmar, R. Goyal, B. Kumar, H. Kumar, Indian J. Chem. B-Organic Chemistry Including Medicinal Chemistry 37 (1998) 941.
156. H.A. Oskooie, M.M. Heravi, A. Sadnia, M. Safarzadegan, F.K. Behbahani, Mendeleev Commun., 17 (2007) 190.
157. J. Krapcho, F.C. Turk, J. Med. Chem. 9 (1966) 191.
158. L.H. Sternback, Angew. Chem. Int. Ed. Engl. 10 (1971) 34.
159. L.O. Randall, B. Kappel, in: S. Garattini, E. Mussini, L.O. Randall (Eds.), Benzodiazepines, Raven Press, New York, 1973, pp. 27-51.
160. H. Schutz, Benzodiazepines, Springer, Heidelberg, 1982.
161. J.A. Herbert, H. Suschitzky, J. Chem. Soc. Perkin I (1974) 2657.
162. H.R. Morales, A. Bulbarela, R. Contreras, Heterocycles 24 (1986) 135.
163. D. Jung, T.W. Choi, Y.Y. Kim, I.S. Kim, Y.M. Park, Y.
164. G. Lee, Synth. Commun. 29 (1999) 1941.
165. M.S. Balakrishna, B. Kaboudin, Tetrahedron Lett. 42 (2001) 1127.
166. M. Curini, F. Epifano, M.C Marcotullio, O. Rosati, Tetrahedron Lett. 42 (2001) 3193.
167. B. Kaboadin, K. Navace, Heterocycles 55 (2001) 1443.
168. M. Pozarentzi, J.S. Stephanatou, C.A. Tsoleridis, Tetrahedron Lett. 43 (2000) 1755.
169. B.M. Reddy, P.M. Sreekanth, Tetrahedron Lett. 44 (2003) 4447.
170. B.P. Bandgar, S.V. Bettigeri, N.S. Joshi, Synth. Commun. 34 (2004) 1447.
171. J.S. Yadav, B.V.S. Reddy, S. P. Kumar, K. Nagaiah, Synthesis (2005) 480.
172. J. S. Yadav, B.V.S. Reddy, N. Lingaiah, P.S. Saiprasad, Synthesis 6 (2004) 901.
173. V. Sivamurugan, K. Deepa, M. Palanichamy, V. Murugesan, Synth. Commun. 34 (2004) 3833.
174. M. Tajbakhsh, M.M. Heravi, B. Mohajerani, A.N. Ahmadi. J. Mol. Cata. A: Chemical 247 (2006) 213.
175. D.V. Jarikote, S.A. Siddiqui, R. Rajagopal, K.V. Srinivasan, Tetrahedron Lett. 44 (2003) 1835.
176. a) J.S. Yadav, B.V.S. Reddy, B. Eshwaraiah, K. Anuradha, Green Chem. 6 (2002) 592;
177. b) D.V. Jarikote, S. Siddiqui, R. Rajagopal, T. Daniel, R.J. Lahoti, K.V. Srinivasan, Tetrahedron Lett. 44 (2003) 1835.
178. M.M. Heravi, V. Zadsirjan, F.K. Behbahani, H.A. Oskooie, J. Mol. Catal. A: Chemical 259 (2006) 201.
179. B. Sazen, D. Sames, Org. Lett. 5 (2003) 3607.
180. J.C. Lewis, S.H. Wiedemann, R.G. Bergman, J.A. Ellman, Org. Lett. 6 (2004) 35.
181. H. Matsushita, S.H. Lee, M. Joung, B. Clapham, K.D. Janda, Tetrahedron Lett. 45 (2004) 313.
182. H.A. Oskooie, M.M. Heravi, A. Sadnia, F.K. Behbahani, F. Jannati, Chinese Chem. Lett. impress.
183. a) B.J. Gaede, L. Mcdermott, J. Heterocycl. Chem. 30 (1993) 49;
184. b) S. Ishii, K. Yagi, T. Umehara, M. Kudo, T. Nawamaki, S. Watanabe, Jap. Pat. 02, 129, 171, 1990; Chem. Abstr. 1990, 113, 172014;
185. C) H. Shimori, T. Ishii, H. Yamazaki, Y. Yanasc, Y. Tanaka, Ger. Pat. 3, 713, 774, 1987; Chem. Abstr. 1988, 108, 112445;
186. d) J.G. Buntaim, L.R. Hatton, D. Hawkins, C.J. Pearson, D.A. Roberts, Eur. Pat. Appl. 295, 117, 1988;
187. Chem. Abstr. 1990, 112, 35845;
188. e) G. Mcazza, G. Zanardi, J. Heterocycl. Chem. 30 (1993) 365.
189. a) N. Hadad, J. Baron, Tetrahedron Lett. 43 (2002) 2171;
190. b) K. Makino, H.S. Kim, Y. Kurasawa, J. Heterocycl. Chem. 35 (1998) 489;
191. c) J. Elguero, Compr. Heterocycl. Chem. II 3 (1996) 1;
192. d) K. Takagi, M. Hubeit-Habart, J. Heterocycl. Chem. 33 (1996) 1003;
193. e) N.R. El-Rayyes, N.A. Al-Awadi, Synthesis (1985) 1028;
194. f) M.P. Sammes, A.R. Katritzky, in: Advances in Heterocyclic Chemistry, Vol. 34, Academic Press, 1983;
195. G) L.C. Behr, R. Fusco, C.H. Jarboe, in: A. Weissberger (Ed.), The Chemistry of Heterocyclic Compounds, Interscience Publishers, John Wiley & Sons, New York, 1967.
196. M.M. Heravi, T. Benmorad, F.K. Behbahani, H.A. Oskooie, Chinese Chem. Soc. Submitted.
197. a) E. Juaristi, Enantioselective Synthesis of α-Amino Acids, Ed., Wiley-VCH, New York, 1997;
198. b) G. Cardillo, C Tomasini, Chem. Soc. Rev. (1996) 117;
199. c) G.I. Georg (Ed.), The Organic Chemistry of α-Lactams, VCH Publishers, New York, 1993;
200. d) F.F. Blicke, Org. React. 1 (1942) 303;
201. e) M. Tramontini, Synthesis (1973) 703;
202. f) M. Tramontini, L. Angiolini, Tetrahedron, 46 (1990) 1791;
203. g) E.F. Kleinman, in: B.M. Trost, I. Fleming (Eds.), Comprehensive Organic Synthesis, Vol. 2, Pergamon, Oxford, 1991, p. 893;
204. h) M. Arend, B. Westermann, N. Risch, Angew. Chem., Int. Ed. 37 (1998) 1044;
205. i) M.E. Jung, in: B.M. Trost, I. Fleming (Eds.), Comprehensive Organic Synthesis, Vol. 4, Pergamon, Oxford, 1991, pp. 30-41 and references therein;
206. j) S. Kobayashi, H. Ishitani, Chem. Rev. 99 (1999) 1069 and references therein.
207. S. Kobayashi, K. Kakumoto, M. Sugiura, Org. Lett. 4 (2002) 1319.
208. a) E.D. Bergmann, D. Ginsburg, R. Pappo, Org. React. 10 (1959) 179;
209. b) D.A. Oare, C.H. Heathcock, in: E.L. Eliel, S.H. Wilen (Eds.), Topics in Stereochemistry, Vol. 19, Wiley Interscience, New York, 1989, pp. 227-407;
210. c) P. Perlmutter, Conjugate Addition Reactions in Organic Synthesis, Tetrahedron Organic Chemistry Series, Vol. 9, Pergamon, Oxford, 1992.
211. J. Christoffers, Eur. J. Org. Chem. (1998) 1259.
212. S.Pelzar, T. Kauf, C. Van Wüllen, J. Christoffers, J. Organometallic Chem. 684 (2003) 308.
213. M. Balogh, I. Hermecz, Z. Meszaros, P. Laszlo, Helv. Chim. Acta. 67 (1984) 2270.
214. J.R. Pfister, Synthesis (1990) 689.
215. A. Maquestiau, A. Mayence, J. Eynde, Tetrahedron Lett. 32 (1991) 3839.
216. J. Eynde, A. Mayence, A. Maquestiau, Tetrahedron 48 (1992) 463.
217. R. Bocker, F.P. Guengerich, J. Med. Chem. 29 (1986) 1596.
218. H. Mashraqui, K.A. Madhavi, Tetrahedron Lett. 39 (1998) 4895.
219. S. Rajender, D.K. Varma, Tetrahedron Lett. 40 (1999) 21.
220. J. Arguello, L.J. Nunez-Vergara, J.C. Sturm, J.A. Squella, Electrochim. Acta. 49 (2004) 4849.
221. C. Lopez-Alarcon, L.J. Nunez-Vergara, J.A. Squella, Electrochim. Acta. 38 (2003) 505.
222. N. Nakamichi, Y. Kawashita, M. Hayashi, Org. Lett. 4 (2002) 3955.
223. a) M.M. Heravi, K. Bakhtiari, H.A. Oskooie, R. Hekmatshoar. Heterocyclic Commun. 12 (2006) 209-212 2006;
224. b) M.M. Heravi, F. Derikvand, H.A. Oskooie, R. Hekmatshoar. J. Chem. Res. (S) (2006) 168;
225. c) L. Fotouhi, S. Khaleghi, M.M. Heravi, Lett. Org. Chem. 3 (2006) 111;
226. d) M.M. Heravi, F. Derikvand, H.A. Oskooie, R. Hekmatshoar. Synth. Commun. 36 (2006) 77;
227. e) M.M. Heravi, F.K. Behbahani, H.A. Oskooie, R. Hekmatshoar. Tetrahedron Letters 46 (2005) 2775;
228. f) M.M. Heravi, M. Ghassemzadeh, Phosphorus Sulfur and Silicon and the Related Elements 180 (2005) 347;
229. g) M.M. Heravi, F. Dirkwand, H.A. Oskooie, M. Ghassemzadeh, Heterocyclic Commun. 11 (2005) 75;
230. h) M.M. Heravi, F.S.S. Moosavi, Y.S. Beheshtiha, M. Ghassemzadeh, Heterocyclic Commun. 10 (2004) 415;
231. i) M.M. Heravi, M. Ghassemzadeh, Heterocyclic Commun. 10 (2004) 465;
232. j) M. Tajbakhsh, M.M. Heravi, A. Hosseini, A. Shahrezaiee, Phosphorus Sulfur and Silicon and the Related Elements 178 (2003) 773;
233. k) Gmelin-Durrer. The Metallurgy of Iron, Vol. 3a, B, Verlag Chemie, 1971.
234. A. Citterio, M.C. Carvajal, A. Mele, M. Nicolini, R. Santi, R. Sebastiano, J. Chem. Soc. Perkin Trans. 2 (1993) 1973.
235. K. Kurachi, H. Kise, Polymer Journal 26 (1994) 1325.
236. K. Nishio, M. Fujimoto, O. Ando, H. Ono, T. Murayama, J. Appl. Electrochem. 26 (1996) 425.
237. G.B. Shulpin, M.M. Bochkova, G.V. Nizova, N.B. Kozlova, Applied Catalysis B-Environmental 12 (1997) 1.
238. X. Zhou, C. Chriswell, Fuel Processing Technology, 46 (1996) 41.
239. G. Mailhot, L. Hykrdová, J. Jirkovský, K. Lemr, G. Grabner, M. Bolte, Applied Catalysis B: Environmental 50 (2004) 25.
240. P. Mazellier, J. Jirkovský, M. Bolte, Pestic. Sci. 49 (1997) 259.
241. N. Brand, G. Mailhot, M. Bolte, Environ. Sci. Technol. 32 (1998) 2715.
242. N. Brand, G. Mailhot, M. Bolte, Chemosphere 40 (2000) 395.
243. G. Mailhot, N. Brand, M. Astruc, M. Bolte, Appl. Organomet. Chem. 16 (2002) 27.
244. C. Catastini, M. Sarakha, G. Mailhot, M. Bolte, Sci. Total Environ. 298 (2002) 219.
245. W. Feng, D. Nansheng, Chemosphere 41 (2000) 1137.
246. A. Strecker, Liebigs Ann. Chem. 75 (1850) 27.
247. P. Biginelli, Ber. Dtsch. Chem. Ges. 24 (1891) 1317.
248. C. Mannich, Kroschl, Arch. Phar. 250 (1912) 647.
249. a) D. Enders, J.P. Shilvock, Chem. Soc. Rev. 29 (2000) 359;
250. b) M. North, in: S.-I. Murahashi (Ed.), Science of Synthesis, Vol. 19, Thieme, Stuttgart, 2004, p. 285.
251. R.O. Duthaler, Tetrahedron 50 (1994) 1539.
252. a) H.A. Oskooie, M.M. Heravi, A. Sadnia, F. Jannati, F.K. Behbahani, Synth. Commun. 37 (2007) 1;
253. b) H.A. Oskooie, M.M. Heravi, K. Bakhtiari, V. Zadsirjan, F.F. Bamoharram, Synlett (2006) 1768.
254. a) M.M. Heravi, H.A. Oskooie, F.K. Behbahani, Russ. J. Org. Chem. Submitted;
255. b) M.M. Heravi, F.K. Behbahani, V. Zadsirjan, H.A. Oskooie, Heterocyclic Commun., 12 (2006) 369;
256. c) M.M. Heravi, K. Bakhtiari, F.F. Bamoharram, Cat. Commun. 7 (2006) 373;
257. d) M.M. Heravi, F.F. Bamoharram, J. Mol. Catal. Chemical 242 (2005) 173;
258. e) M. Tajbakhsh, M.M. Heravi, A.N. Ahmadi, J. Mol. Catal. Chemical 236 (2005) 216.
259. C.O. Kappe, J. Org. Chem. 62 (1997) 7201.