DOI: 10.1039/C4RA06772J
RSC Advances
Franck, B. Figadère, R. Hocquemiller, A. Fournet,
Antimicrob. Agents Chemother. 2005, 49:4950–4956.
36 P.M. Loiseau, G. Suman, V. Aditya, S. Saumya, S. K. Puri, F.
Sliman, N. -B.Marie, D. Desmaele, Antimicrob. Agents
Chemother. 2011, 55, 1777-1780;
37. V. S. Gopinath, J. Pinjari, T.D. Ravindra, V. Aditya, V.
Preeti, S. Rahul, M. Manjunath, P. S. K. Goud, R. Vikram, P.
Bose, M.V.S. Rao, G. Suman, S. K. Puri, D. Launay, D.
Martin, Eur. J. Med. Chem, 2013, 69, 527-536;
10 38 L. T. Phan, T. Jian, Z. Chen, Y. –L. Qiu, Z. Wang, T. Beach,
A. Polemeropoulos, Y. S. Or, J. Med. Chem. 2004, 47, 2965-
2968;
39.J. Chevalier, S. Atifi, A. Eyraud, A. Mahamoud, J. Barbe, J. –
M.. Pages, J. Med. Chem. 2001, 44, 4023-4026;
15 40. K. –C. Fang, Y. –L. Chen, J. –Y. Sheu, T. –C. Wang, C. -C.
Tzeng, J. Med. Chem. 2000, 43, 3809-3812;
41.S. J. Benkovic, S. J. Baker, M. R. K. Alley, Y. –H. Woo, Y. –
K. Zhang, T. Akama, W. Mao, J. Baboval, P. T. R.
Rajagopalan, M. Wall, L. S. Kahng, A. Tavassoli, L. Shapiro,
L. J. Med. Chem. 2005, 48, 7468-7476.
42 J. F. Mouscadet, D. Desmae¨le, Molecules 2010, 15, 3048-
3078;
43. J. Polanski, H. Niedbala, R. Musiol, D. Tabak, B. Podeszwa,
R. Gieleciak, A. Bak, A. Palka, T. Magdziarz, Acta Poloniae
Pharm. Drug Res. 2004, 61, 3;
44 J. Polanski, F. Zouhiri, L. Jeanson, D. Desmaele, J. d’Angelo,
J. Mouscadet, R. Gieleciak, J. Gasteiger, M. Le Bret, J. Med.
Chem. 2002, 45, 4647
45 .J. Polanski, H. Niedbala, R. Musiol, B. Podeszwa, D. Tabak,
A. Palka, A. Mencel, J. F. Mouscadet, M. Le Bret, Lett.
Drugs Des. Disc. 2007, 4, 99.
46 F. Zouhiri, J. F. Mouscadet, K. Mekouar, D. Desmaele, D.
Savoure, H. Leh, F. Subra, M. L. Bret, C. Auclair, J.
d’Angelo, J. Med. Chem, 2000, 43, 1533–1540.
35 47 .J. Polanski, H. Niedbala, R. Musiol, B. Podeszwa, D. Tabak,
A. Palka, A. Mencel, J. Finster, J. F. Mouscadet, M. Le Bret,
Lett. Drugs Des. Disc. 2006, 3, 175;
48. C. Bailly, W. Laine, B. Baldeyrou, M. –C. De Pauw-
Gillet, P. Colson, C. Houssier, K. Cimanga, S. V.
Miert, A. J. Vlietinck, L. Pieters, Anti-Cancer Drug
Des. 2000, 15, 191-201;
49. L. Dassonneville, K. Bonjean, M.- C. De Pauw-Gillet, P.
Colson, C. Houssier, J. Quetin-Leclercq, L. Angenot, S. Y.
Ablordeppey,. Bioorg. Med. Chem. 2002, 10, 1337–1346;
61. F. Jin, X.Y. Jin, Y.L. Jin, D.W. Sohn, S-A. Kim, D.H. Sohn,
Y.C.Kim, H.S. Kim, Arch.Pharm.Res. 2007, 30, 1359-1367;
b) N. Yaulì, O. Üçüncü, E. Aydìn, Y.Gök, A. Yaar, C. N.Baltacì,
Yìldìrìm, M. Küçük, J.Photochem. Photobiol. A: Chem. 2005,
75 169, 229.
62. S. Mostahar, P. Katun, A. Islam, J.Biol.Sci., 2007, 7 (3), 514-
519; b) S. Katade, U. Phalgune, S Biswas, R. Wakharkar, N.
Deshpande, Indian J.Chem., 2008, 47B, 927-931
63. Z. Nowakowka, Eur J Med Chem, 2007, 42, 125-137.
80 64.T. Narender, K.P. Reddy, Tetrahedron Lett. 2007, 48, 3177;
b) N.O. Calloway, L.D. Green, J. Am. Chem. Soc. 1937, 59, 809;
c) L. Mazza, A. Guaram, Synthesis (1980) 41;d) N. Iranpoor, F.
Kazemi, Tetrahedron 1998, 54 9475.
65. C. N. Khobragade, R. G. Bodade, M. S. Shine, R. R. Deepa,
85 R. B. Bhosale, B S. Dawane, Enzym Inhib Med. Chern., 2008, 3,
341-346.
5
66. M. Balasubramanian, J.G. Keay, A.R Katritzky, C.W. Rees,
E.F.V. Scriven (Eds.), Comprehensive Heterocyclic
Chemistry II, Vol. 5Pergamon Press, Oxford (1996), pp. 167–
20
25
30
90
243
67. C.-C. Cheng, S.-J. Yan, Org. React., 1982, 28, 37–200
68. G. Jones A. Weiss Berger, A.C. Taylor (Eds.), The
Chemistry of Heterocyclic Compounds, Vol. 32Wiley, New
York Chapter 2, 1977, 93
95 69. X. Zhang, M.A. Campo, T. Yao, R.C. Larock, Org. Lett.,
2005, 7, 763
70. B.R. McNaughton, B.L. Miller, Org. Lett., 2003, 5, 4257
71. J.S. Yadav, B.V.S. Reddy, P. Sreedhar, R.S. Rao, K.
Nagaiah, Synthesis 2004, 2381
100 72.T. Demaude, L. Knerr, P. Pasau J. Comb. Chem., 2004, 6, 768
73. A. M. Farghaly, N. S. Habib, M. A. Khalil, O. A. El-Sayed,
A. E. Bistawroos, Archiv der Pharmazie, 1990, 323, 247–251
74. C. Patteux, V. Levacher, G. Dupas, Org. Lett., 2003, 5, 3061
75. N.S. Mani, P. Chen, T.K. Jones, J. Org. Chem., 1999, 64,
105
6911–6914
76. Elderfield, R.C. Heterocyclic compounds. John-Wiley &
Sons: New York, 1960, Vol. 4. pp. 6-59.
77.(a) J. Marco-Contelles, E. P´erez-Mayoral, A. Samadi, M. C.
Carreiras and E. Soriano, Chem. Rev., 2009, 109, 2652–2671; (b)
40
110 S. A. Yamashkin and E. A. Oreshkina, Chem. Heterocycl.
Compd., 2006, 42, 701–718
78.a) B. Crousse, J.-P. Bégué, D. Bonnet-Delpon,. Tetrahedron
Lett., 1998, 39, 5765-5768, b) B. Crousse, J.-P. Bégué, D.
Bonnet-Delpon, J. Org. Chem.,2000, 65, 5009-5013.
115 79. Y. Makioka, T. Shindo, Y. Taniguchi, K. Takaki, Fujiwara,
Y. Synthesis, 1995, 801-806.
45 50 L. Dassonneville, A. Lansiaux, A. Wattelet, N. Wattez, C.
Mahieu, S. Van Miert, L. Pieters, C. Bailly, Eur. J.
Pharmacol. 2000, 409, 9-18;
51. C. Bailly, Biochemistry 1999, 38, 7719-7726;
52. B. D. Lee, Z. Li, K. J. French, Y. Zhuang, Z. Xia, C. D.
50 Smith, J. Med. Chem. 2004, 47, 1413–1422.
53 O. Bilker, V. Lindo, M. Panico, A. E. Etiene, T. Paxton, A.
Dell, M. Rogers, R. E. Sinden, H. R. Morris, Nature 1998,
392, 289-292;
80. C.K Cho, B. Hooh, S.C. Shim, J. Heterocycl. Chem., 1999,
36, 1175-1178.
81. a)C. S. Cho, D. T. Kim, T.-J. Kim and S. C. Shim, Bull.
120 Korean Chem. Soc., 2003, 24, 1026–1028; (b) C.S Cho, B. H. Oh
and S. C. Shim, J. Heterocycl. Chem., 1999, 36, 1175–1178.b) C.
S; c)Cho, B. H. Oh, J. S. Kim, T.- J.Kim and S. C. Shim,
Chem.Commun., 2000, 1885–1886.
54 M. Matsugi, F. Tabusa, J. Minamikawa, Tetrahedron Lett.,
55
2000, 41, 8523; c) J. Ziegler, R. Linck, D. W. Wright, Curr.
Med. Chem, 2001, 8, 171;
55 . S. Khatib, O. Narya, R. Musa, M. Shmuel, S. Tamir, J. Vaya,
Bioorg. Med. Chem. 2005, 13, 433.b) V. Opletalova, Cesk. Slov.
Farm. 2000, 49, 278-284.
60 56 a)J. Aponte, M. Verastegui, E. Malaga, M. Zimic, M.
Quiliano, A. J. Vaisberg, R.H. Gilman, G.B. Hammond, J. Med.
Chem. 2008, 51, 6230-6234;b) A. Shah, A. M Khan, R. Qureshi,
F.L. Ansari, F.M. Nazar, S.S. Shah, Int. J. Mol. Sci. 2008, 9,
1424-1434.
82. H. Aramoto, Y. Obora and Y. Ishii, J. Org. Chem., 2009, 74,
125 628–633.
83 . B.S. Jayashreem Sameer arora, K.N. Venugopala, Asian J.
Chem. 2008, 20, 1-7.
84. N T. Patil, F. Nawaz Khan, Y. Yamamoto, Tetrahedron Lett.
2004, 45,8497.
130 85.Y. Isogai, F. Nawaz Khan, N. Asao, Tetrahedron 2009, 65,
9575.
86.K. Prabakaran, F. Nawaz Khan, J. S. Jin, Tetrahedron Lett.
2011, 52, 2566.
87. R. Subashini, FRN. Khan, Monatsh.Chem. 2012, 143, 485
135 88.SM. Roopan, FRN. Khan, Med. Chem. Res. 2011, 20,732
89.V Krishnakumar, F Nawaz Khan, BK. Mandal , E D Jeong,
Tetrahedron Lett. 2014, in press
65 57 K.Prabakaran, P.Manivel, F. Nawaz Khan, Tetrahedron Lett.
2010, 51,4340
58 Y. –L. Chen, K. –C. Fang, J. –Y. Sheu, S. –L. Hsu, C. –C.
Tzeng, J. Med. Chem. 2000, 44, 2374-2377;
59. B. M. I. Newton, N. White, Annu. Rev. Med. 1999, 50, 179;
70 60 P. A. Winstanley, Parasitol. Today 2000, 16, 146–153
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