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RSC Advances
Page 4 of 5
DOI: 10.1039/C5RA21270G
COMMUNICATION
Journal Name
Acknowledgement
Leblanc, R. G. Ball, C. Brideau, C. C. Chan, N. Chauret, W.
Cromlish, D. Ethier, J. Y. Gauthier, R. Gordon, G. Greig, J.
Guay, S. Kargman, C. K. Lau, G. O’Neil, J. Silva, M. Thérien,
C. vanstaden, E. Wong, L. Xu and P. Prasit, Bioorg. Med.
Financial support from CSIR and UGC New Delhi for the
research grant to M. Muneer and funding from the National
Science Foundation, USA (MRI, CHE-0420497) for the purchase
of the Apex-II diffractometer for the research group of N. P.
Rath are gratefully acknowledged. The authors are highly
thankful to Prof. Gautam R. Desiraju (IISC Bangalore) for
providing single crystal diffraction facility. Tariq A. Shah thanks
University Grants Commission New Delhi for providing UGC-
BSR (JRF) Fellowship.
Chem. Lett., 1997, 7, 57; (d) H. M. Ashour, O. G. Shaaban,
O. H. Rizk and I. M. El-Ashmawy, Euro. J. Med. Chem.
2013, 62, 341; (e) P. Karegoudar, D. J. Prasad, M. Ashok,
M. Mahalinga, B. Poojary and B. S. Holla, Eur. J. Med.
Chem., 2008, 43, 808; (f) B. Cox, P. Healy, M. S. Nobbs and
G. P. Shah, U. S. Patent 6, 2002, 465, 461.
(15) (a) R. Lesyk, O. Vladzimirska, S. Holota, L. Zaprutko and A.
Gzella, Eur. J. Med. Chem., 2007, 42, 641; (b) C. F. Beyer,
N. Zhang, R. Hernandez, D. Vitale, J. Lucas, T. Nguyen, C.
Discafani, S. Ayral-Kaloustian and J. Gibbons, J. Cancer
Research, 2008, 68, 2292; (c) A. Husain, M. Rashid, M.
Shaharyar, A. A. Siddiqui and R. Mishra, Eur. J. Med.
Chem., 2013, 62, 785.
Notes and references
(1) A. R. Katritzky, A. Pastor and M. Voronkov, Org. Lett., 2000,
2, 429.
(2) R. Pignatello, S. Mazzone, A. M. Panico, G. Mazzone, G.
Pennisi, R. Castana, M. Matera and G. Blandino. Eur. J.
Med. Chem., 1991, 26, 929.
(16) (a) R. Gujjar, A. Marwaha, F. El Mazouni, J. White, K. L.
White, S. Creason, D. M. Shackleford, J. Baldwin, W. N.
Charman, F. S. Buckner, S. Charman, P. K. Rathod and M.
A. Phillips, J. Med. Chem., 2009, 52, 1864; (b) A. Marwaha,
J. White, F. El Mazouni, S. A. Creason, S. Kokkonda, F. S.
Buckner and P. K. Rathod, J. Med. Chem., 2012, 55, 7425.
(17) S. Demirayak, G. Zitouni, P. Chevallet, K. Erol and F. S.
Kilic,. Farmaco., 1993, 48, 707.
(3) J. F. Riou and J. P. Hénichart, Bioorg. Med. Chem. Lett.,
2009, 19, 3434.
(4) F. Montel, C. Lamberth and P. M. J. Jung, Tetrahedron,
2008, 64, 6372.
(5) R. A. Serey, R. Torres and B. A. Latorre. Cienc. Inv. Agr.,
2007, 34, 215.
(6) (a) N. Zhang, S. Ayral-Kaloustian, T. Nguyen, J. Afragola, R.
Hernandez, J. Lucas, J. Gibbons and C. Beyer .J. Med.
Chem., 2007, 50, 319; (b) N. Zhang, S. Ayral- Kaloustian, T.
Nguyen, R. Hernandez and C. Beyer, Bioorg. Med. Chem.
Lett., 2007, 17, 3003.
(18) (a) V. M. Dianov, I. G. Chikaeva, G. A. Timirkhanova, Y. V.
Strokin, F. S. Zarudiy and V. A. Lifanov, Khim.-Farm. Zh.,
1994, 28, 555; (b) R. Houssin, N. Helbecque, J. L Bernier
and J. P. Henichart, J. Biomol. Struct. Dyn., 1986,
4, 219; (c)
(7) K. S. Bhat, B. Poojary, D. J. Prasad, P. Naik and B. S. Holla,
Eur. J. Med. Chem., 2009, 44, 5066.
E. Ohler, H. S. Kang and E. Zbiral. Chem. Ber., 1988, 121
,
977; (d) Y. Tamura, H. Hayashi, E. Saeki, J. H. Kim and M.
Ikeda, J. Heterocycl. Chem., 1974, 11, 459.
(8) Y. A. Al-Soud, N. A. Al-Masoudi, R. Loddo and P. L. Colla,
Arch. Pharm. Chem. Life Sci., 2008, 34, 365.
(19) E. B. Erkhitueva, A. V. Dogadina, A. V. Khramchikhin and B.
I. Ionin, Tetrahedron Lett., 2012, 53, 4304.
(9) (a) I. Simiti, and A. Marie, Rev. Roum. Chim., 1982, 27, 273;
(b) P. Puthiyapurayil, B. Poojary, C. Chikkanna and S. K.
Buridipad, Eur. J. Med. Chem., 2012, 57, 407.
(10) (a) H. A. H. El-Sherif, A. M. Mahmoud, A. A. O. Sarhan, Z.
(20) F. Montel, C. Lamberth and P. M. J. Jung, Tetrahedron,
2008, 64, 6372.
(21) (a) Z. Xie. X. Zhu, Y. Guan, D. Zhu, H. Hu, C. Lin, Y. Pan, J.
Jiang and L. Wang, Org. Biomol. Chem., 2013, 11, 1390; (b)
K. T. Potts and S. Husain, J. Org. Chem., 1971, 36, 10; (c) N.
D. Heindel and J. R. Reid, J. Org. Chem., 1980, 45, 2479; (d)
A. Hozien and O. M. A. Habib, J. Sulfur Chem.,2006, 27
,
65; (b) M. S. Karthikeyan, Eur. J. Med. Chem. 2009, 44
,
827; (c) L. Yin, Z. Shuai, L. Zhi-Jun and Z. Hai-Liang, Euro.
J. Med. Chem., 2013, 64, 54; (d) A. Abdel-Aziem, M. S. El-
T. Sasaki, E. Ito and I. Shimizu, J. Org. Chem., 1982, 47
,
,
Gendy and A. O Abdelhamid, Euro. J. Chem., 2012, 3,
2757; (e) G. Jones and H. Ollivierre, Tetrahedron, 1991, 47
455; (e) M. K. Khera, I. A. Cliffe, T. Mathur and O.
Prakash, Bioorg. & Med. Chem. Lett., 2011, 21, 2887; (f)
T. Karabasanagouda, A. V. Adhikari and N. S. Shetty, Eur.
J. Med. Chem., 2007, 42, 521.
2851; (f) A. R. Katritzky, A. Pastor and M. Voronkov, Org.
Lett., 2000, , 429; (g) M. M. Heravi and A. Kivanloo,
Tetrahedron Lett., 2005, 46, 1607; (h) K. M. Al-Zaydi, R. M.
Borik and M. H. Elnagdi, Molecules, 2003, , 910; (i) E. I.
2
8
(11) (a) B. S. Holla, K. N. Poojary, B. Kalluraya and P. V Gowda,
Farmaco., 1996, 51, 793; (b) Q. Chen, X. L . Zhu, Z. M. Liu,
et al. Euro. J. Med. Chem., 2008, 43, 595.
Al-Afaleq, Synthetic Communication. 2000, 30, 1985; (j) Y.
Tominag, S. Sakai, S. Kohra, J. Tsuka, Y. Matsuda and G.
Kobayashi, Chem. Pharm. Bull. 1985, 33, 962.
(12) D. Takiguchi, T. Sato and S. Nomura, Chem. Abstr., 1987,
106, 138456.
(22) N. A. Mir, T. A. Shah, S. Ahmad, M. Muneer, N. P. Rath and
M. Ahmad, Tetrahedron Lett., 2014, 55, 1706.
(13) (a) M. S. Karthikeyan, Eur. J. Med. Chem., 2009, 44, 827;
(b) S.P. Aytaç, B. Tozkoparan, F. B. Kaynak and G. Aktay,
Eur. J. Med. Chem., 2009, 44, 4528.
(14) (a) B. Berk, G. Aktay, E. Yesilada and M. Ertan, Pharmazie,
2001, 56, 613; (b) R. Pignatello, S. Mazzone, A. M. Panico,
G. Mazzone, G. Pennisi, R. Castana, M. Matera and G.
Blandino, Eur. J. Med. Chem., 1991, 26, 929; (c) P. Roy, Y.
4 | J. Name., 2012, 00, 1-3
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