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催化学报  2011 

CobaltNanoparticlesPromotedHighlyEfficientOnePotFour-ComponentSynthesisof1,4-DihydropyridinesunderSolvent-FreeConditions

DOI: 10.1016/S1872-2067(10)60295-1, PP. 1850-1855

Keywords: cobaltnanoparticle,1,4-dihydropyridine,four-componentcondensation,heterogeneoucatalyst,magneticallyseparablecatalyst

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Abstract:

?AstraightforwardandgeneralmethodhasbeendevelopedforthesynthesisofC5-unsubstitiuted1,4-dihydropyridinesbyareactionusingdimedone,acetophenone,aromaticaldehydes,andammoniumacetateinthepresenceofacatalyticamountofConanoparticlesasaheterogeneousandeco-friendlycatalystwithhighcatalyticactivityatroomtemperatureundersolvent-freeconditions.Thiscatalystiseasilyseparatedbymagneticdevicesandcanbereusedwithoutanyapparentlossofactivityforthereaction.Inaddition,itisveryinterestingthatwhenusingConanoparticlesasacatalyst,spatially-hinderedaldehydessuchas2-methoxy-,2-fluoro-,and2-chloro-aldehydesaresuitableforthisreaction.

References

[1]  afari J, Khalili S D, Rezaei M, Banitaba S H, Meshkani F. Monatsh Chem, 2010, 141: 1339
[2]  eng Q, Yang Y, Yuan Y. J Mol Catal A, 2004, 219: 175
[3]  u H, Li M, Chen H, Li X. J Mol Catal A, 2006, 259: 156
[4]  aulik F E. Catal Rev, 1972, 6: 49
[5]  eller M, Cornils B, Frohning C D, Kohlpaintner C W. J Mol Catal A, 1995, 104: 17
[6]  ngvary F. Coord Chem Rev, 2007, 251: 2087
[7]  en F, B?nnemann H, Jiang J, Lu D, Wang Y, Jin Z. Appl Or-ganomet Chem, 2005, 19: 81
[8]  russ A J, Gelesky M A, Machado G, Dupont J. J Mol Catal A, 2006, 252: 212
[9]  Suzuki I, Suzumura Y, Takeda K. Tetrahedron Lett, 2006, 47: 7861
[10]  Shaabani A, Bazgir A, Teimouri F. Tetrahedron Lett, 2003, 44: 857
[11]  Li M, Zuo Z, Wen L, Wang S. J Comb Chem, 2008, 10: 436
[12]  Sabitha G, Reddy G S K, Reddy C S, Yadav J S. Tetrahedron Lett, 2003, 44: 4129
[13]  Wang L M, Sheng J, Zhang L, Han J W, Fan Z Y, Tian H, Qian C T. Tetrahedron, 2005, 61: 1539
[14]  Ji S, Jiang Z Q, Lu J, Loh T P. Synlett, 2004: 831
[15]  Tu S J, Yan S, Cao X D, Wu S S, Zhang X H, Hao W J, Han Z G, Shi F J. Organomet Chem, 2009, 649: 91
[16]  a L, Peng Q, He D. Catal Lett, 2009, 130: 137
[17]  Anastas P T, Warner J C. In: Green Chemistry: Theory and Practice. Oxford: Oxford University Press, 1998
[18]  Kalinski C, Lemoine H, Schmidt J, Burdack C, Kolb J, Um-kehrer M, Ross G. Synlett, 2008: 4007
[19]  Debache A, Ghalem W, Boulcina R, Belfaitah A, Rhouati S, Carboni B. Tetrahedron Lett, 2009, 50: 5248
[20]  Klusa V. Drugs Future, 1995, 20: 135
[21]  Bretzel R G, Bollen C C, Maeser E, Federlin K F. Am J Kidney Dis, 1993, 21(6s3): 53
[22]  Bretzel R G, Bollen C C, Maeser E, Federlin K F. Drugs Fu-ture, 1992, 17: 465
[23]  Rainer B, Volker G. Drugs Future, 1995, 20: 499
[24]  Janis R A, Triggle D J. J Med Chem, 1983, 26: 775
[25]  Boecker R H, Guengerich F P. J Med Chem, 1986, 29: 1596
[26]  Gaudio A C, Korolkovas A, Tkahata Y. J Pharm Sci, 1994, 83: 1110
[27]  Gordeev M F, Patel D V, Gordon E M. J Org Chem, 1996, 61: 924
[28]  Svetlik J, Veizerova L, Kittmann V. Tetrahedron Lett, 2008, 49: 3520
[29]  Heravi M M, Bakhtiri K, Javadi N M, Bamoharram F F, Saeedi M, Oskooi H A. J Mol Catal A, 2007, 264: 50
[30]  Cherkupally S R, Mekalan R. Chem Pharm Bull, 2008, 56: 1002
[31]  Sainani J B, Shah A C, Arya V P. Indian J Chem Sect B, 1994, 33B: 526
[32]  Kumar A, Maurya R A. Tetrahedron Lett, 2007, 48: 3887
[33]  Ko S, Yao C F. Tetrahedron, 2006, 62: 7293
[34]  Zang H, Zhang Y, Zang Y, Cheng B-W. Ultrason Sonochem, 2010, 17: 495
[35]  Tu S J, Zhou J F, Deng X, Cai P J, Wang H, Feng J C. Chin J Org Chem, 2001, 21: 313
[36]  Wang X S, Shi D Q, Tu S J. Synth Commun, 2002, 32: 3449
[37]  Chen W Y, Lu J, Jin J R. Lett Org Chem, 2006, 3: 317
[38]  Kim S W, Son S U, Lee S S, Hyeon T, Chung Y K. Chem Commun, 2001: 2212
[39]  Safari J, Banitaba S H, Khalili S D. J Mol Catal A, 2011, 335: 46
[40]  Guo F, Zheng H, Yang Z, Qian Y. Mater Lett, 2002, 56: 906

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