Recent advances in InCl3-catalyzed one-pot organic synthesis

Tetrahedron

Volumn 68, Issue 42, 2012, Pages 8683-8697

  Singh, Maya Shankar ^a   Raghuvanshi, Keshav ^a  

^a BANARAS HINDU UNIVERSITY   (India)

Author keywords

Catalysis; Indium trichloride; Multicomponent reactions; Organic synthesis; Solvent free conditions

Indexed keywords

CARBONYL DERIVATIVE; CHROMENE DERIVATIVE; COUMARIN DERIVATIVE; INDIUM CHLORIDE; INDOLE DERIVATIVE; PHOSPHONIC ACID DERIVATIVE; PYRIMIDINONE DERIVATIVE; QUINOLINE DERIVATIVE; SCHIFF BASE;

ALDOL REACTION; ARTICLE; CATALYSIS; CATALYST; CHEMICAL BOND; CHEMICAL MODIFICATION; CHEMICAL REACTION; CHEMICAL STRUCTURE; COMPLEX FORMATION; DRUG SYNTHESIS; ENANTIOSELECTIVITY; MUKAIYAMA REACTION; ONE POT SYNTHESIS; PRIORITY JOURNAL; REACTION OPTIMIZATION; REDUCTION; SYNTHESIS;

EID: 84865730848     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.06.099     Document Type: Review

References (227)

1. J.S. Yadav, A. Antony, J. George, and B.V.S. Reddy Curr. Org. Chem. 14 2010 414
2. J.S. Yadav, A. Aneesh, G. Jimil, and B.V.S. Reddy Eur. J. Org. Chem. 2010 591
3. T.-P. Loh, and G.L. Chua Chem. Commun. 2006 2739
4. J. Podlech, and T.C. Maier Synthesis 2003 633
5. V. Nair, S. Ros, C.N. Jayan, and B.S. Pillai Tetrahedron 60 2004 1959
6. B.C. Ranu Eur. J. Org. Chem. 2000 2347
7. J. Auge, N. Lubin-Germain, and J. Uziel Synthesis 2007 1739
8. T.-P. Loh, and L.L. Wei Synlett 1998 975
9. T.-P. Loh, K.C. Xu, D.S.C. Ho, and K.Y. Sim Synlett 1998 369
10. J. Song, Z.H. Hua, S. Qi, S.J. Ji, and T.-P. Loh Synlett 2004 829
11. T.-P. Loh, and X.R. Li Angew. Chem., Int. Ed. 36 1997 980
12. T.-P. Loh, and X.R. Li Chem. Commun. 1996 1929
13. X.R. Li, and T.-P. Loh Tetrahedron: Asymmetry 7 1996 1535
14. T.-P. Loh, and X.R. Li Eur. J. Org. Chem. 1999 1893
15. Z.L. Shen, and T.-P. Loh Org. Lett. 9 2007 5413
16. Z.L. Shen, H.L. Cheong, and T.-P. Loh Chem. - Eur. J. 14 2008 1875
17. Z.L. Shen, Y.L. Yeo, and T.-P. Loh J. Org. Chem. 73 2008 3922
18. I. Ugi Pure Appl. Chem. 73 2001 187
19. J. Zhu, and H. Bienayme Multicomponent Reactions 2005 Wiley-VCH Weinheim, Germany
20. A. Domling Chem. Rev. 106 2006 17
21. D.M. D'Souza, and T.J.J. Mueller Chem. Soc. Rev. 36 2007 3169
22. C.C.A. Cariou, G.J. Clarkson, and M. Shipman J. Org. Chem. 73 2008 9762
23. A. Alizadeh, F. Movahedi, and A.A. Esmaili Tetrahedron Lett. 47 2006 4469
24. A. Dömling, and I. Ugi Angew. Chem., Int. Ed. 39 2000 3168
25. D.J. Ramon, and M. Yus Angew. Chem., Int. Ed. 44 2005 1602
26. D. Tejedor, and F. Garcia-Tellado Chem. Soc. Rev. 36 2007 484
27. J. Zhu Eur. J. Org. Chem. 2003 1133
28. N.R. Candeias, F. Montalbano, P.M.S.D. Cal, and P.M.P. Gois Chem. Rev. 110 2010 6169
29. A.V. Artemev, N.K. Gusarova, S.F. Malysheva, V.I. Mamatyuk, Y.V. Gatilov, I.A. Ushakov, and B.A. Trofimov Eur. J. Org. Chem. 2010 6157
30. L. Banfi, A. Basso, L. Giardini, R. Riva, V. Rocca, and G. Guanti Eur. J. Org. Chem. 2011 100
31. K. Wang, D. Kim, and A. Dömling J. Comb. Chem. 12 2010 111
32. A. Basso, L. Banfi, R. Riva, and G. Guanti J. Org. Chem. 70 2005 575
33. S.T. Staben, and N. Blaquiere Angew. Chem., Int. Ed. 49 2010 325
34. I. Akritopoulou-Zanze Curr. Opin. Chem. Biol. 12 2008 324
35. T. Yue, M.-X. Wang, D.-X. Wang, G. Masson, and J. Zhu J. Org. Chem. 74 2009 8396
36. B.A. Trofimov, L.V. Andriyankova, K.V. Belyaeva, A.G. Malkina, L.P. Nikitina, A.V. Afonin, and I.A. Ushakov Eur. J. Org. Chem. 2010 1772
37. N. Ma, B. Jiang, G. Zhang, S.-J. Tu, W. Wever, and G. Li Green Chem. 12 2010 1357
38. X.-H. Duan, X.-Y. Liu, L.-N. Guo, M.-C. Liao, W.-M. Liu, and Y.-M. Liang J. Org. Chem. 70 2005 6980
39. S.-J. Tu, B. Jiang, R.-H. Jia, J.-Y. Zhang, Y. Zhang, C.-S. Yao, and F. Shi Org. Biomol. Chem. 4 2006 3664
40. H.-L. Wei, Z.-Y. Yan, Y.-N. Niu, G.-Q. Li, and Y.-M. Liang J. Org. Chem. 72 2007 8600
41. S.-L. Cui, J. Wang, and Y.-G. Wang Org. Lett. 9 2007 5023
42. S.-L. Cui, J. Wang, and Y.-G. Wang Org. Lett. 10 2008 1267
43. X.-H. Chen, W.-Q. Zhang, and L.-Z. Gong J. Am. Chem. Soc. 130 2008 5652
44. N. Li, X.-H. Chen, J. Song, S.-W. Luo, W. Fan, and L.-Z. Gong J. Am. Chem. Soc. 131 2009 15301
45. X.-Y. Guan, L.-P. Yang, and W.-H. Hu Angew. Chem., Int. Ed. 49 2010 2190
46. C.L. Floch, E.L. Gall, E. Léonel, J. Koubaa, T. Martens, and P. Retailleau Eur. J. Org. Chem. 2010 5279
47. A. Strecker Liebigs Ann. Chem. 75 1850 27
48. A. Hantzsch Liebigs Ann. Chem. 215 1882 1
49. P. Biginelli Gazz. Chim. Ital. 23 1893 360
50. N.A. Petasis, and I. Akritopoulou Tetrahedron Lett. 34 1993 583
51. I. Ugi, R. Meyr, R. Fetzer, and C. Steinbruckner Angew. Chem. 71 1959 386
52. I. Ugi, and C. Steinbrückner Chem. Ber. 94 1961 734
53. C. Hulme, and V. Gore Curr. Med. Chem. 10 2003 51
54. J.D. Sunderhaus, C. Dockendorff, and S.F. Martin Org. Lett. 9 2007 4223
55. R.W. Armstrong, A.P. Combs, P.A. Tempest, S.D. Brown, and T.A. Keating Acc. Chem. Res. 29 1996 123
56. C. Haurena, E.L. Gall, S. Sengmany, T. Martens, and M. Troupel J. Org. Chem. 75 2010 2645
57. B. Willy, and T.J.J. Muller Eur. J. Org. Chem. 2008 4157
58. M. Adib, E. Sheikhi, A. Kavoosi, and H.R. Bijanzadeh Tetrahedron 66 2010 9263
59. W.-B. Chen, Z.-J. Wu, Q.-L. Pei, L.-F. Cun, X.-M. Zhang, and W.-C. Yuan Org. Lett. 12 2010 3132
60. I. Ugi J. Prakt. Chem. 339 1997 499
61. P. Eilbracht Chem. Rev. 99 1999 3329
62. L. Weber Curr. Med. Chem. 9 2002 1241
63. R.E. Dolle, and K.H. Nelson J. Comb. Chem. 1 1996 235
64. L.A. Thompson, and J.A. Ellman Chem. Rev. 96 1996 555
65. I. Ugi, B. Werner, and A. Domling Molecules 8 2003 53
66. D.E. Fogg, and E.N. dos Santos Coord. Chem. Rev. 248 2004 2365
67. G. Poli, and G. Giambastiani J. Org. Chem. 67 2002 9456
68. G. Balme, E. Bossharth, and N. Monteiro Eur. J. Org. Chem. 2003 4101
69. M. Malacria Chem. Rev. 96 1996 289
70. P.J. Parsons, C.S. Penkett, and A.J. Shell Chem. Rev. 96 1996 195
71. L.F. Tietze Chem. Rev. 96 1996 115
72. J.M. Lee, Y. Na, H. Han, and S. Chang Chem. Soc. Rev. 33 2004 302
73. J.C. Wasilke, S.J. Obrey, R.T. Baker, and G.C. Bazan Chem. Rev. 105 2005 1001
74. M.J. Climent, A. Corma, and S. Iborra ChemSusChem 2 2009 500
75. M.J. Climent, A. Corma, and S. Iborra Chem. Rev. 111 2011 1072
76. M.S. Singh, and S. Chowdhury RSC Adv. 2 2012 4547
77. A.L. Braga, P.H. Schneider, M.W. Paixao, A.M. Deobald, C. Peppe, and D.P. Bottega J. Org. Chem. 71 2006 4305
78. A.L. Braga, P.H. Schneider, M.W. Paixao, and A.M. Deobald Tetrahedron Lett. 47 2006 7195
79. C.G. Frost, and J.P. Hartley Mini-Rev. Org. Chem. 1 2004 1
80. Z.-H. Zhang Synlett 2005 711
81. Y.-U. Teo, J.-D. Goh, and T.-P. Loh Org. Lett. 7 2005 2743
82. J. Lu, S.-J. Ji, Y.-U. Teo, and T.-P. Loh Org. Lett. 7 2005 159
83. J.A. Marshall, and K.W. Hinkle J. Org. Chem. 60 1995 1920
84. S. Harada, S. Handa, S. Matsunaga, and M. Shibasaki Angew. Chem. 117 2005 4439
85. Angew. Chem., Int. Ed. 44 2005 4365
86. R. Yanada, S. Obika, Y. Kobayashi, T. Inokuma, M. Oyama, K. Yanada, and Y. Takemoto Adv. Synth. Catal. 347 2005 1632
87. R. Yanada, S. Obika, M. Oyama, and Y. Takemoto Org. Lett. 6 2004 2825
88. Y. Onishi, D. Ogawa, M. Yasuda, and A. Baba J. Am. Chem. Soc. 124 2002 13690
89. M. Yasuda, Y. Onishi, M. Ueba, T. Miyai, and A. Baba J. Org. Chem. 66 2001 7741
90. Y.-C. Teo, and T.-P. Loh Org. Lett. 7 2005 2539
91. G. Babu, and P.T. Perumal Tetrahedron Lett. 39 1998 3225
92. T.-P. Loh, J. Pei, and M. Lin Chem. Commun. 1996 2315
93. G. Babu, and P.T. Perumal Tetrahedron Lett. 38 1997 5025
94. G. Babu, and P.T. Perumal Tetrahedron 55 1999 4793
95. G. Babu, R. Nagarajan, R. Natarajan, and P.T. Perumal Synthesis 2000 611
96. A. Srinivasa, K.M. Mahadevan, and V. Hulical Synth. Commun. 39 2008 93
97. T. Miyai, Y. Onishi, and A. Baba Tetrahedron Lett. 39 1998 6291
98. T. Miyai, Y. Onishi, and A. Baba Tetrahedron 55 1999 1017
99. B.C. Ranu, S.S. Dey, and S. Samanta Arkivoc iii 2005 44
100. T.-P. Loh, and L.L. Wei Tetrahedron Lett. 39 1998 323
101. T. Mukaiyama, T. Ohno, J.S. Han, and S. Kobayashi Chem. Lett. 1991 949
102. S. Kobayashi, T. Busujima, and S. Nagayama Tetrahedron Lett. 39 1998 1579
103. T.-P. Loh, G.-L. Chua, J.J. Vittal, and M.-W. Wong Chem. Commun. 1998 861
104. T.-P. Loh, J. Pei, K.S. Koh, G.-Q. Cao, and X.-R. Li Tetrahedron Lett. 38 1997 3465
105. T.-P. Loh, J.M. Huang, S.H. Goh, and J.J. Vittal Org. Lett. 2 2000 1291
106. D.S. Bose, A.P. Rudradas, and M. Hari Babu Tetrahedron Lett. 43 2002 9195
107. G.K. Friestad, C.S. Korapala, and H. Ding J. Org. Chem. 71 2006 281
108. Y. Onishi, T. Ito, M. Yasuda, and A. Baba Eur. J. Org. Chem. 2002 1578
109. M. Bandini, P.M. Giorgio Cozzi, A. Melchiorre, and A. Umani-Ronchi Tetrahedron Lett. 42 2001 304
110. M.A. Ceschi, L.A. Felix, and C. Peppe Tetrahedron Lett. 41 2000 9695
111. M. Bandini, P.M. Giorgio Cozzi, P.M. Giocomini, S. Selva, and A. Umani-Ronchi J. Org. Chem. 67 2002 3700
112. J.S. Yadav, B.V.S. Reddy, A.K. Raju, and C.V. Rao Tetrahedron Lett. 43 2002 5437
113. J.S. Yadav, and B.V.S. Reddy Synthesis 2002 511
114. J.S. Yadav, B.V.S. Reddy, A.D. Krishna, and T. Swamy Tetrahedron Lett. 44 2003 6055
115. G. Babu, and P.T. Perumal Aldrichimica Acta 33 2000 14
116. T.-P. Loh, J. Pei, and G.-Q. Cao Chem. Commun. 1996 1819
117. T. Hirashita, T. Kamei, T. Horie, H. Yamamura, M. Kawai, and S. Araki J. Org. Chem. 64 1999 172
118. P. Thirumurugan, and P.T. Perumal Tetrahedron 65 2009 7620
119. G. Babu, and P.T. Perumal Tetrahedron 54 1998 1627
120. G. Babu, R. Nagarajan, and P.T. Perumal Synthesis 2000 661
121. M. Hadden, and P.J. Stevenson Tetrahedron Lett. 40 1999 1215
122. P. Jayashree, G. Shanthi, and P.T. Perumal Synlett 2009 917
123. G. Shanthi, and P.T. Perumal Tetrahedron Lett. 50 2009 3959
124. K. Ren, M. Wang, and L. Wang Org. Biomol. Chem. 7 2009 4858
125. S. Kobayashi Synlett 1994 689
126. R.W. Marshman Aldrichimica Acta 28 1995 77
127. S. Kobayashi Eur. J. Org. Chem. 15 1950 5
128. S. Kobayashi Chem. Lett. 1991 2187
129. F.A. Cotton, and G. Wilkinson Advanced Inorganic Chemistry 5th ed. 1988 Wiley New York, NY p 973
130. S. Kobayashi, M. Sugiura, H. Kitagawa, and W.W.-L. Lam Chem. Rev. 102 2002 2227
131. P. Cintas Synlett 1995 1087
132. C.-J. Li, and T.-H. Chan Tetrahedron 55 1999 11149
133. K.K. Chauhan, and C.G. Frost J. Chem. Soc., Perkin Trans. 1 2000 3015
134. F. Fringuelli, O. Piermatti, F. Pizzo, and L. Vaccaro Curr. Org. Chem. 7 2003 1661
135. G.K. Verma, K. Raghuvanshi, R. Kumar, and M.S. Singh Tetrahedron Lett. 53 2012 399
136. G.C. Nandi, S. Samai, R. Kumar, and M.S. Singh Tetrahedron Lett. 50 2009 7220
137. S. Samai, G.C. Nandi, R. Kumar, and M.S. Singh Tetrahedron Lett. 50 2009 7096
138. S. Chowdhury, G.C. Nandi, S. Samai, and M.S. Singh Org. Lett. 13 2011 3762
139. R. Takita, Y. Fukuta, R. Tsuji, T. Ohshima, and M. Shibasaki Org. Lett. 7 2005 1363
140. D.S. Rampon, R. Giovenardi, T.L. Silva, R.S. Rambo, A.A. Merlo, and P.H. Schneider Eur. J. Org. Chem. 2011 7066
141. Y. Zhang, P. Li, M. Wang, and L. Wang J. Org. Chem. 74 2009 4364
142. B.C. Ranu, A. Hajra, and U. Jana Org. Lett. 1 1999 1141
143. E. Elamparuthi, M. Anniyappan, D. Muralidharan, and P.T. Perumal Arkivoc xi 2005 6
144. B. Pal, V.S. Giri, and P. Jaisankar Catal. Commun. 6 2005 711
145. G. Babu, N. Sridhar, and P.T. Perumal Synth. Commun. 30 2000 1609
146. B. Montaignac, M.R. Vitale, V. Ratovelomanana-Vidal, and V. Michelet J. Org. Chem. 75 2010 8322
147. Y.-L. Xu, Y.-M. Pan, Q. Wu, H.-S. Wang, and P.-Z. Liu J. Org. Chem. 76 2011 8472
148. K.C. Chunavala, and S. Adimurthy Synth. Commun. 41 2011 1843
149. Z.-L. Shen, S.-J. Ji, and T.-P. Loh Tetrahedron 64 2008 8159
150. S.-S. Chua, A. Alni, L.-T.J. Chan, M. Yamane, and T.-P. Loh Tetrahedron 67 2011 5079
151. S. Källström, and R. Leino Bioorg. Med. Chem. 16 2008 601
152. E.F. Kleinmann Comprehensive Organic Synthesis 1991 Pergamon New York, NY
153. T.-P. Loh, and S.-L. Chen Org. Lett. 4 2002 3647
154. A.R. Hajipour, L. Khazdooz, and A. Zarei Synth. Commun. 41 2011 2200
155. T.-P. Loh, S.B.K.W. Liung, K.-L. Tan, and L.-L. Wei Tetrahedron 56 2000 3227
156. J.S. Yadav, B.V.S. Reddy, G. Satheesh, G. Narasimhulu, Y. Portier, C. Madhavi, and A.C. Kunwar Tetrahedron Lett. 49 2008 3341
157. E. Yamuna, M. Zeller, K. Jayarampillai, and R. Prasad Tetrahedron Lett. 52 2011 6805
158. P.R. Krishna, Y.L. Prapurna, and M. Alivelu Tetrahedron Lett. 52 2011 3460
159. B. Li, G. Wang, Z. Li, and X. Meng Tetrahedron Lett. 52 2011 3891
160. S.K. Das, J. Roy, K.A. Reddy, and C. Abbineni Carbohydr. Res. 338 2003 2237
161. M. Ramesh, P.S. Moham, and P. Shanmugam Tetrahedron 40 1984 4041
162. N.B. Perry, J.W. Blunt, J.D. McCombs, and M.H.G. Munro J. Org. Chem. 51 1986 5476
163. N.M. Williamson, P.R. March, and A.D. Ward Tetrahedron Lett. 36 1995 7721
164. J.V. Johnson, S. Rauckman, P.D. Baccanari, and B. Roth J. Med. Chem. 32 1989 1942
165. R.W. Caling, P.D. Leeson, A.M. Moseley, R. Baker, A.C. Foster, S. Grimwood, J.A. Kemp, and G.R. Marshall J. Med. Chem. 35 1992 1942
166. R.W. Carling, P.D. Leeson, A.M. Moseley, J.D. Smith, K. Saywell, M.D. Trickelbank, J.A. Kemp, G.R. Marshall, A.C. Foster, and S. Grimwood Bioorg. Med. Chem. Lett. 3 1993 65
167. A.R. Katritzky, S. Rachwal, and B. Rachwal Tetrahedron 52 1996 15031
168. L.S. Povarov Russ. Chem. Rev. (Engl. Transl.) 36 1967 656
169. D.L. Boger, and S.M. Weinreb Hetero Diels-Alder Methodology in Organic Synthesis 1987 Academic San Diego, CA Chapters 2 and 9
170. J. Zhang, and C.-J. Li J. Org. Chem. 67 2002 3969
171. S. Hatakeyama, N. Ochi, H. Numata, and S. Takano J. Chem. Soc., Chem. Commun. 1988 1202
172. R. González, N. Martín, C. Seoane, J.L. Marco, A. Albert, and F.H. Cano Tetrahedron Lett. 33 1992 3809
173. K. Urbahns, E. Horváth, J.-P. Stasch, and F. Mauler Bioorg. Med. Chem. Lett. 13 2003 2637
174. B.S. Jensen, D. Strobaek, S.P. Olesen, and P. Christophersen Curr. Drug Targets 2 2001 401
175. R. Kohler, H. Wulff, I. Eichler, M. Kneifel, D. Neumann, A. Knorr, I. Grgic, D. Kampfe, H. Si, J. Wibawa, R. Real, K. Borner, S. Brakemeier, H.D. Orzechowski, H.P. Reusch, M. Paul, K.G. Chandy, and J. Hoyer Circulation 108 2003 1119
176. A.P. Dobbs, and S. Martinovic Tetrahedron Lett. 43 2002 7055
177. A.P. Dobbs, S.J.J. Guesne, S. Martinovic, S.J. Coles, and M.B. Hursthouse J. Org. Chem. 68 2003 7880
178. B.C. Ranu, and U. Jana J. Org. Chem. 63 1998 8212
179. J.A. Joule, and K. Mills Heterocyclic Chemistry 4th ed. 2006 Blackwell Science Oxford 170
180. H.-X. Xu, and S.F. Lee Phytother. Res. 15 2001 39
181. K.C. Fylaktakidou, D.J. Hadjipavlou-Litina, K.E. Litinas, and D.N. Nicolaides Curr. Pharm. Des. 10 2004 3813
182. J.R. Hwu, R. Singh, S.C. Hong, Y.H. Chang, A.R. Das, I. Vliegen, E. De Clercq, and J. Neyts Antivir. Res. 77 2008 157
183. S. Sardari, Y. Mori, K. Horita, R.G. Micetich, S. Nishibe, and M. Daneshtalab Bioorg. Med. Chem. 7 1999 1933
184. D. Egan, P. James, D. Cooke, and R. O'Kennedy Cancer Lett. 118 1997 201
185. P. Valenti, A. Rampa, M. Recanatini, A. Bisi, F. Belluti, P. Da Re, M. Carrara, and L. Cima Anti-Cancer Drug Des. 12 1997 443
186. C. Spino, M. Dodier, and S. Sotheeswaran Bioorg. Med. Chem. Lett. 8 1998 3475
187. B.V.S. Reddy, M.R. Reddy, G. Narasimhulu, and J.S. Yadav Tetrahedron Lett. 51 2010 5677
188. R. Kumar, K. Raghuvanshi, R.K. Verma, and M.S. Singh Tetrahedron Lett. 51 2010 5933
189. G.C. Nandi, S. Samai, and M.S. Singh Synlett 2010 1133
190. G.C. Nandi, S. Samai, R. Kumar, and M.S. Singh Tetrahedron 65 2009 7129
191. G.K. Verma, K. Raghuvanshi, R.K. Verma, P. Dwivedi, and M.S. Singh Tetrahedron 67 2011 3698
192. T.-P. Loh, and L.-L. Wei Tetrahedron 54 1998 7615
193. B.A. Keay, and P.W. Dibble A.R. Katritzky, C.W. Rees, E.F. Schriven, C.W. Bird, Comprehensive Heterocyclic Chemistry II Vol. 2 1996 Pergamon Oxford, UK 395
194. S. Dey, D. Nandi, P.K. Pradhan, V.S. Giri, and P. Jaisankar Tetrahedron Lett. 48 2007 2573
195. B.C. Ranu, A. Hajra, S.S. Dey, and U. Jana Tetrahedron 59 2003 813
196. B.C. Ranu, A. Hajra, and U. Jana Tetrahedron Lett. 41 2000 531
197. R. Kumar, G.C. Nandi, R.K. Verma, and M.S. Singh Tetrahedron Lett. 51 2010 442
198. R.D.H. Murray, J. Mendez, and S.A. Brown The Natural Coumarins: Occurrences, Chemistry and Biochemistry 1982 John Wiley and Sons New York, NY, USA
199. J.D. Hepworth, C.D. Gabbutt, and B.M. Heron A.R. Katritzky, C.W. Rees, E.F.V. Scriven, Comprehensive Heterocyclic Chemistry II Vol. 5 1996 Pergamon New York, NY 417
200. J.M. Hamilton miller Antimicrob. Agents Chemother. 39 1995 2375
201. H. Madari, D. Panda, L. Wilson, and R.S. Jacobs Cancer Res. 63 2003 1214
202. G. Finn, B. Creaven, and D. Egan Eur. J. Pharmacol. 481 2003 159
203. G.J. Finn, B.S. Creaven, and D.A. Egan Cancer Lett. 214 2004 43
204. G.J. Finn, B.S. Creaven, and D.A. Egan Eur. J. Pharm. Sci. 26 2005 16
205. M. Basanagouda, K. Shivashankar, M.V. Kulkarni, V.P. Rasal, H. Patel, S.S. Mutha, and A.A. Mohite Eur. J. Med. Chem. 45 2010 1151
206. R.K. Verma, G.K. Verma, K. Raghuvanshi, and M.S. Singh Tetrahedron 67 2011 584
207. G. Shanthi, and P.T. Perumal Tetrahedron Lett. 48 2007 6785
208. B.C. Ranu, A. Hajra, and U. Jana J. Org. Chem. 65 2000 6270
209. B. Das, K. Damodar, and N. Bhunia J. Org. Chem. 74 2009 5607
210. F. Fringuelli, F. Pizzo, S. Tortoioli, and L. Vaccaro Org. Lett. 7 2005 4411
211. Y.S. Cho, H.Y. Kim, J.H. Cha, A.N. Pae, H.Y. Koh, J.H. Choi, and M.H. Chang Org. Lett. 4 2002 2025
212. R. Hayashi, and G.R. Cook Org. Lett. 9 2007 1311
213. Y.-S. Yang, Z.-L. Shen, and T.-P. Loh Org. Lett. 11 2009 2213
214. J.S. Yadav, B.V. Subba Reddy, and S.K. Pandey Synth. Commun. 32 2002 715
215. B.C. Ranu, S. Bhadra, and L. Adak Tetrahedron Lett. 49 2008 2588
216. A.K. Chakraborti, and R. Gulhane Tetrahedron Lett. 44 2003 6749
217. M. Weïwer, and E. Dunach Tetrahedron Lett. 47 2006 287
218. S. Muthusamy, S.A. Babu, and C. Gunanathan Tetrahedron Lett. 42 2001 359
219. S. Sengupta, and S. Mondal Tetrahedron Lett. 41 2000 6245
220. G. Shanthi, G. Subbulakshmi, and P.T. Perumal Tetrahedron 63 2007 2057
221. J.S. Yadav, A. Sunny, B.V.S. Reddy, and G. Sabitha Tetrahedron Lett. 42 2001 8063
222. J.S. Yadav, B.V.S. Reddy, G. Sabitha, A. Prabhakar, and A.C. Kunwar Tetrahedron Lett. 44 2003 2221
223. H.S.P. Rao, and S. Sivakumar J. Org. Chem. 71 2006 8715
224. H.-J. Yuan, M. Wang, Y.-J. Liu, and Q. Liu Adv. Synth. Catal. 351 2009 112
225. R.K. Verma, G.K. Verma, G. Shukla, and M.S. Singh RSC Adv. 2 2012 2413
226. S. Samai, G.C. Nandi, and M.S. Singh Tetrahedron 68 2012 1247
227. Y.-L. Xu, Y.-M. Pan, P. Liu, H.-S. Wang, X.-Y. Tian, and G.-F. Su J. Org. Chem. 77 2012 3557