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催化学报  2014 

Thioureadioxide:Anefficientandreusableorganocatalystfortherapidone-potsynthesisofpyrano[4,3-b]pyranderivativesinwater

DOI: 10.1016/S1872-2067(12)60727-X, PP. 127-133

Keywords: Pyrano[4,3-b]pyran,Thioureadioxide,4-Hydroxy-6-methylpyran-2-one,One-potsynthesis

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Abstract:

?Aseriesofpyrano[4,3-b]pyranderivativeshavebeensynthesizedinexcellentyieldsbythereactionofaromaticaldehydeswithmalononitrileorcyanoacetateand4-hydroxy-6-methylpyran-2-oneinwaterat80℃,withthetransformationbeingcatalyzedbyanaqueoussolutionofthioureadioxide(TUD).Uponcompletionofthereaction,theproductwasisolatedbyfiltrationorextractionandtheremainingaqueousTUDsolutioncouldbereusedseveraltimeswithoutanydiscernibleimpactonitscatalyticactivity.Thisprocedureoffersseveraladvantagesoverexistingprocedures,includinghighyields,operationalsimplicity,theuseofanon-toxiccatalystandsolvent,shortreactiontimeandminimumpollutionoftheenvironment,makingitausefulandattractiveprocessforthepreparationofpyrano[4,3-b]pyranderivatives.

References

[1]  Domling A, Ugi I. Angew Chem, Int Ed, 2000, 39: 3168
[2]  Heck S, Domling A. Synlett, 2000: 424
[3]  Martinez-Grau A, Marco J L. Bioorg Med Chem Lett, 1997, 7: 3165
[4]  Hiramoto K, Nasuhara A, Michikoshi K, Kato T, Kikugawa K. Mutat Res, 1997, 395: 47
[5]  Venkatesham A, Rao R S, Nagaiah K, Yadav J S, Roopa-Jones G, Basha S J, Sridhar B, Addlagatta A. Med Chem Comm, 2012, 3: 652
[6]  Bianchi G, Tava A. Agric Biol Chem, 1987, 51: 2001
[7]  Salvi P P, Mandhare A M, Sartape A S, Pawar D K, Han S H, Kolekar S S. C R Chim, 2011, 14: 878
[8]  Rajguru D, Keshwal B S, Jain S. Med Chem Res, 2013, doi: 10.1007/s00044-013-0586-4
[9]  Verma S, Kumar S, Jain S L, Sain B. Org Biomol Chem, 2011, 9: 6943
[10]  Kumar S, Jain S L, Sain B. RSC Advances, 2012, 2: 789
[11]  Verma S, Jain S L. Tetrahedron Lett, 2012, 53: 6055
[12]  Ohura O, Fujimoto O. US Patent 4 233 238. 1980
[13]  Ghashang M, Mansoor S S, Aswin K. J Adv Res, 2013, doi: 10.1016/j.jare.2013.03.003
[14]  Ghashang M, Mansoor S S, Aswin K. Res Chem Intermed, 2013, doi: 10.1007/s11164-013-1419-2
[15]  Davoodnia A, Khashi M, Tavakoli-Hoseini N. Chin J Catal (催化学报), 2013, 34: 1173
[16]  Azizi N, Davoudpour A, Eskandari F, Batebi E. Monatsh Chem, 2013, 144: 405
[17]  Makawana J A, Patel M P, Patel R G. Arch Pharm (Weinheim). 2012, 345: 314
[18]  Mohr S J, Chirigos M A, Fuhrman F S, Pryor J W. Cancer Res, 1975, 35: 3750
[19]  Kamdar N R, Haveliwala D D, Mistry P T, Patel S K. Euro J Med Chem, 2010, 45: 5056
[20]  Hazeri N, Maghsoodlou M T, Mousavi M R, Aboonajmi J, Sa-farzaei M. Res Chem Intermed, 2013, doi: 10.1007/s11164-013-1179-z
[21]  Nasseri M A, Sadeghzadeh S M. Monatsh Chem, 2013,144: 1551
[22]  Khurana J M, Kumar S. Tetrahedron Lett, 2009, 50: 4125
[23]  Pratap U R, Jawale D V, Netankar P D, Mane R A. Tetrahedron Lett, 2011, 52: 5817
[24]  Hasaninejad A, Shekouhy M, Golzar N, Zare A, Doroodmand M M. Appl Catal A, 2011, 402: 11
[25]  Wang X S, Zeng Z S, Li Y L, Shi D Q, Tu S J, Zhou J X. ARKIVOC, 2006: 107
[26]  Rajguru D, Keshwal B S, Jain S, Bhagwat V W. Monatsh Chem, 2013, doi: 10.1007/s00706-013-0975-x
[27]  Mirza-Aghayan M, Saravani F, Tarlani A A, Abaee M S, Boukher-roub R. Monatsh Chem, 2013, doi: 10.1007/s00706-013- 1035-2
[28]  Ghashang M, Aswin K, Mansoor S S. Res Chem Intermed, 2013, doi: 10.1007/s11164-013-1027-1
[29]  Mansoor S S, Aswin K, Logaiya K, Sudhan P N, Malik S. Res Chem Intermed, 2012, doi: 10.1007/s11164-012-1008-9

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