Chinese Journal of Catalysis ›› 2015, Vol. 36 ›› Issue (5): 728-733.DOI: 10.1016/S1872-2067(14)60307-7
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Nader Ghaffari Khaligh, Sharifah Bee Abd Hamid
Received:
2015-01-07
Revised:
2015-01-29
Online:
2015-04-17
Published:
2015-04-17
Contact:
Nader Ghaffari Khaligh
Nader Ghaffari Khaligh, Sharifah Bee Abd Hamid. 4-(Succinimido)-1-butane sulfonic acid as a Brönsted acid catalyst for the synthesis of pyrano[4, 3-b]pyran derivatives using thermal and ultrasonic irradiation[J]. Chinese Journal of Catalysis, 2015, 36(5): 728-733.
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URL: https://www.cjcatal.com/EN/10.1016/S1872-2067(14)60307-7
[1] De Clercq E. Farmaco, 1999, 54: 26 [2] Parreira R L T, Abrahão O, Galembeck S E. Tetrahedron, 2001, 57: 3243 [3] Presti E L, Boggia R, Feltrin A, Menozzi G, Dorigo P, Mosti L. Farmaco, 1999, 54: 465 [4] Anderson W K, Dean D C, Endo T. J Med Chem, 1990, 33: 1667 [5] Rajguru D, Keshwal B S, Jain S. Med Chem Res, 2013, 22: 5934 [6] Dragovich P S, Prins T J, Zhou R, Brown E L, Maldonado F C, Fuhrman S A, Zalman L S, Tuntland T, Lee C A, Patick A K, Matthews D A, Hendrickson T F, Kosa M B, Liu B, Batugo M R, Gleeson J P R, Sakata S K, Chen L J, Guzman M C, Meador J W III, Ferre R A, Worland S T. J Med Chem, 2002, 45: 1607 [7] Kemnitzer W, Kasibhatla S, Jiang S C, Zhang H, Zhao J H, Jia S J, Xu L F, Crogan-Grundy C, Denis R, Barriault N, Vaillancourt L, Charron S, Dodd J, Attardo G, Labrecque D, Lamothe S, Gourdeau H, Tseng B, Drewe J, Cai S X. Bioorg Med Chem Lett, 2005, 15: 4745 [8] Kemnitzer W, Drewe J, Jiang S C, Zhang H, Wang Y, Zhao J H, Jia S J, Herich J, Labreque D, Storer R, Meerovitch K, Bouffard D, Rej R, Denis R, Blais C, Lamothe S, Attardo G, Gourdeau H, Tseng B, Kasibhatla S, Cai S X. J Med Chem, 2004, 47: 6299 [9] Kemnitzer W, Drewe J, Jiang S C, Zhang H, Zhao J H, Crogan-Grundy C, Xu L F, Lamothe S, Gourdeau H, Denis R, Tseng B, Kasibhatla S, Cai S X. J Med Chem, 2007, 50: 2858 [10] Fan X S, Feng D, Qu Y Y, Zhang X Y, Wang J J, Loiseau P M, Andrei G, Snoeck R, Clercq E D. Bioorg Med Chem Lett, 2010, 20: 809 [11] Tatsuta K, Yamaguchi T, Tsuda Y, Yamaguchi Y, Hattori N, Nagai H, Hosokawa S. Tetrahedron Lett, 2007, 48: 4187 [12] Tanabe K, Hölderich W F. Appl Catal A, 1999, 181: 399 [13] Cole-Hamilton D J. Science, 2003, 299: 1702 [14] Chakrabarti A, Sharma M M. React Polym, 1993, 20: 1 [15] Riego J M, Sedin Z, Zaldivar J M, Marziano N C, Tortato C. Tetrahedron Lett, 1996, 37: 513 [16] Turro N J. Tetrahedron, 1987, 43: 1589 [17] Zolfigol M A, Chehardoli G, Dehghanian M, Niknam K, Shirini F, Khoramabadi-Zad A. J Chin Chem Soc, 2008, 55: 885 [18] Weber U S, Steffen B, Siegers C P. Res Commun Mol Pathol Pharmacol, 1998, 99: 193 [19] Du B X, Yin M Y, Zhang M M, Li Y L, Wang X S. J Heterocycl Chem, 2012, 49: 1439 [20] Patil A D, Freyer A J, Eggleston D S, Haltiwanger R C, Bean M F, Taylor P B, Caranfa M J, Breen A L, Bartus H R, Johnson R K, Hertzberg R P, Westley J W. J Med Chem, 1993, 36: 4131 [21] Anastas P T, Warner J C. Green Chemistry: Theory and Practice. Oxford: Oxford Univ Press, 1998 [22] Mason T J. Ultrason Sonochem, 2007, 14: 476 [23] Khaligh N G, Shirini F. Ultrason Sonochem, 2013, 20: 26 [24] Khaligh N G. Ultrason Sonochem, 2013, 20: 1062 [25] Cravotto G, Cintas P. Chem Soc Rev, 2006, 35: 180 [26] Xia M, Lu Y D. Ultrason Sonochem, 2007, 14: 235 [27] Shirini F, Khaligh N G. Phosphorus Sulfur Silicon Relat Elem, 2011, 186: 2156 [28] Shirini F, Khaligh N G. Dyes Pigm, 2012, 95: 789 [29] Shirini F, Khaligh N G. Chin J Catal (催化学报), 2013, 34: 695 [30] Shirini F, Khaligh N G. Chin J Catal (催化学报), 2013, 34: 1890 [31] Suslick K S, Didenko Y, Fang M M, Hyeon T, Kolbeck K J, McNamara W B III, Mdleleni M M, Wong M. Philos Trans R Soc A, 1999, 357: 335 [32] Mason T J, Peters D. Practical Sonochemistry: Power Ultrasound Uses and Applications. 2nd Ed. Chichester: Horwood Publishing, 2002. 17 [33] Luche J L. Synthetic Organic Sonochemistry. New York: Plenum Press, 1998 [34] Jin T S, Sun G, Li Y W, Li T S. Green Chem, 2002, 4: 255 [35] Piao M Z, Imafuku K. Tetrahedron Lett, 1997, 38: 5301 [36] Magedov I V, Manpadi M, Ogasawara M A, Dhawan A S, Rogelj S, Van Slambrouck S, Steelant W F A, Evdokimov N M, Uglinskii P Y, Elias E M, Knee E J, Tongwa P, Antipin M Y, Kornienko A. J Med Chem, 2008, 51: 2561 [37] Stoyanov E V, Ivanov I C, Heber D. Molecules, 2000, 5: 19 [38] Shi D Q, Niu L H, Zhuang Q Y. Chin J Org Chem (史达清, 牛力惠, 庄启亚. 有机化学), 2008, 28: 1633 [39] Wang X S, Zeng Z S, Li Y L, Shi D Q, Tu S J, Zhou J X. Arkivoc, 2006, (11): 107 [40] Shaabani A, Samadi S, Badri Z, Rahmati A. Catal Lett, 2005, 104: 39 [41] Shaabani A, Samadi S, Rahmati A. Synth Commun, 2007, 37: 491 [42] Seifi M, Sheibani H. Catal Lett, 2008, 126: 275 [43] Rajguru D, Keshwal B S, Jain S. Chin Chem Lett, 2013, 24: 1033 [44] Khaligh N G. Monatsh Chem, 2014, 145: 1643 [45] Ghashang M, Mansoor S S, Aswin K. Chin J Catal (催化学报), 2014, 35: 127 |
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