[Et3NH][HSO4]-catalyzed one-pot, solvent-free synthesis and biological evaluation of α-amino phosphonates
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  • 作者:Mubarak H. Shaikh ; Dnyaneshwar D. Subhedar…
  • 关键词:Ionic liquid ; α ; Aminophosphonate ; Antifungal ; Antioxidant ; ADME prediction
  • 刊名:Research on Chemical Intermediates
  • 出版年:2016
  • 出版时间:May 2016
  • 年:2016
  • 卷:42
  • 期:5
  • 页码:5115-5131
  • 全文大小:1,997 KB
  • 参考文献:1.Z. Lei, C. Dai, B. Chen, Chem. Rev. 114, 1289 (2014)CrossRef
    2.M.V. Fedorov, A.A. Kornyshev, Chem. Rev. 114, 2978 (2014)CrossRef
    3.X.X. Han, H. Du, C.T. Hung, L.L. Liu, P.H. Wu, D.H. Ren, S.J. Huang, S.B. Liu, Green Chem. 17, 499 (2015)CrossRef
    4.Z.N. Siddiqui, K. Khan, ACS Sustain. Chem. Eng. 2, 1187 (2014). (reference cited their in) CrossRef
    5.L.D. Quin, G.S. Quin, A Guide to Organophosphorus Chemistry (Wiley, New York, 2000)
    6.D.E.C. Corbridge, Phosphorus Chemistry, Biochemistry and Technology (Elsevier, Amsterdam, 2000)
    7.R. Engel, Chem. Rev. 77, 349 (1977)CrossRef
    8.R.A. Lerner, S.J. Benkovic, P.G. Schultz, Science 252, 659 (1991)CrossRef
    9.M.R. Saidi, N. Azizi, Synlett 8, 1347 (2002)CrossRef
    10.M. Sienczyk, J. Oleksyszyn, Curr. Med. Chem. 16, 1673 (2009)CrossRef
    11.K. Panigrahi, M.J. Eggen, J.H. Maeng, Q. Shen, D.B. Berkowitz, Chem. Biol. 16, 928 (2009)CrossRef
    12.R. Hirschmann, A.B. Smith, C.M. Taylor, P.A. Benkovic, S.D. Taylor, K.M. Yager, P.A. Sprengler, S. Venkovic, J. Sci. 265, 234 (1994)CrossRef
    13.R. Ghosh, S. Maiti, A. Chakraborty, D. Maiti, J. Mol. Cat. Chem. 53, 210 (2004)
    14.P.P. Sun, Z.X. Hu, Z.H. Huang, Synth. Commun. 34, 4293 (2004)CrossRef
    15.Z.P. Zhan, J.P. Li, Synth. Commun. 35, 2501 (2005)CrossRef
    16.A.S. Paraskar, A. Sudalai, Arkivoc X, 183 (2006)
    17.K.S. Ambica, S.C. Taneja, M.S. Hundal, K.K. Kapoor, Tetrahedron Lett. 49, 2208 (2008)CrossRef
    18.B.C. Ranu, A. Hajra, U. Jana, Org. Lett. 1, 1141 (1999)CrossRef
    19.J.S. Yadav, B.V.S. Reddy, S. Raj, K.B. Reddy, A.R. Prasad, Synthesis 15, 2277 (2001)CrossRef
    20.J.S. Yadav, B.V.S. Reddy, P. Sreedhar, Green Chem. 4, 436 (2002)CrossRef
    21.S. Lee, J.K. Lee, C.E. Song, D.C. Kim, Bull. Korean Chem. Soc. 23, 667 (2002)CrossRef
    22.Z. Zhou, Y. Pei, L. Wu, Org. Chem. Int. (2012). doi:10.​1155/​2012/​375656
    23.S.A. Sadaphal, S.S. Sonar, A.H. Kategaonkar, M.S. Shingare, Bull. Korean Chem. Soc. 30, 1054 (2009)CrossRef
    24.S. Lee, J.H. Park, J. Kang, J.K. Lee, Chem. Commun. 1698 (2001)
    25.S.A. Dake, D.S. Raut, K.R. Kharat, R.S. Mhaske, S.U. Deshmukh, R.P. Pawar, Bioorg. Med. Chem. Lett. 21, 2527 (2011)CrossRef
    26.K. Manabe, S. Kobayashi, Chem. Commun. 669 (2000)
    27.S. Chandrasekhar, C. Narsihmulu, S.S. Sultana, B. Saritha, S.J. Prakash, Synlett 4, 505 (2003)CrossRef
    28.J. Zou, Pol. J. Chem. 55, 643 (1981)
    29.S. Laschat, H. Kunz, Synthesis 90 (1992)
    30.M.M. Kabachnik, T.N. Ternovskaya, E.V. Zobnina, I.P. Beletskaya, Russ. J. Org. Chem. 38, 480 (2002)CrossRef
    31.M.M. Kabachnik, E.V. Zobnina, I.P. Beletskaya, Russ. J. Org. Chem. 41, 505 (2005)CrossRef
    32.T. Akiyama, M. Sanada, K. Fuchibe, Synlett 10, 1463 (2003)CrossRef
    33.B. Kaboudin, E. Jafari, Synlett 12, 1837 (2008)CrossRef
    34.N. Azizi, F. Rajabi, M.R. Saidi, Tetrahedron Lett. 45, 9233 (2004)CrossRef
    35.S. Bhagat, A.K. Chakraborti, J. Org. Chem. 72, 1263 (2007)CrossRef
    36.H. Firouzabadi, N. Iranpoor, S. Sobhani, Synthesis 16, 2692 (2004)CrossRef
    37.A. Elmakssoudi, M. Zahouily, A. Mezdar, A. Rayadh, S. Sebti, Comptes Rendus Chim. 8, 1954 (2005)CrossRef
    38.S. Bhagat, A.K. Chakraborti, J. Org. Chem. 73, 6029 (2008)CrossRef
    39.J. Weng, C. Wang, H. Li, Y. Wang, Green Chem. 8, 96 (2006)CrossRef
    40.P.V. Shinde, A.H. Kategaonkar, B.B. Shingate, M.S. Shingare, Tetrahedron Lett. 52, 2889 (2011)CrossRef
    41.K.S. Niralwad, B.B. Shingate, M.S. Shingare, Ultra. Sonochem. 17, 760 (2010)CrossRef
    42.S.S. Sonar, S.A. Sadaphal, N.V. Shitole, N.R. Jogdand, B.B. Shingate, M.S. Shingare, Bull. Korean Chem. Soc. 30, 1711 (2009)CrossRef
    43.S. Lee, J.H. Park, J. Kang, J.K. Lee, Chem. Commun. 1698 (2001)
    44.C. Qian, T. Huang, J. Org. Chem. 63, 4125 (1998)CrossRef
    45.X.J. Mu, M.Y. Lei, J.P. Zou, W. Zhang, Tetrahedron Lett. 47, 1125 (2006)CrossRef
    46.B. Karmakar, S. Paul, J. Banerji, Arkivoc ii, 161 (2011)
    47.R. Ghosh, S. Maiti, A. Chakraborty, D.J. Maiti, Mol. Catal. A: Chem. 210, 53 (2004)CrossRef
    48.M. Xia, Y.D. Lu, Ultra. Sonochem. 14, 235 (2007)CrossRef
    49.B.C. Ranu, A. Hajra, Green Chem. 4, 551 (2002)CrossRef
    50.M.H. Sarvari, Tetrahedron 64, 5459 (2008)CrossRef
    51.R.K. Reddy, A. Vijender, P. Krishnaiah, G. Venkataramana, V.L. Reddy, Venkateswarlu. Synth. Commun. 34, 1677 (2004)CrossRef
    52.X.Y. Lv, J.M. Zhang, C.H. Xing, W.Q. Du, S.Z. Zhu, Synth. Commun. 37, 743 (2007)CrossRef
    53.M. Zahouily, A. Elmakssoudi, A. Mezdar, A. Rayadh, S. Sebti, Catal. Commun. 8, 225 (2007)CrossRef
    54.S. Chandrasekhar, S.J. Prakash, V. Jagadeswar, C. Narsihmulu, Tetrahedron Lett. 42, 5561 (2001)CrossRef
    55.H.C. Kolb, M.G. Finn, K.B. Sharpless, Angew. Chem. Int. Ed. 40, 2004 (2001)CrossRef
    56.V.V. Rostovtsev, L.G. Green, V.V. Fokin, K.B. Sharpless, Angew. Chem. Int. Ed. 41, 2596 (2002)CrossRef
    57.C.W. Tornoe, C. Christensen, M. Meldal, J. Org. Chem. 67, 3057 (2002)CrossRef
    58.C. Arkona, J. Rademann, Angew. Chem. Int. Ed. 52, 8210 (2013)CrossRef
    59.P. Ertl, B. Rohde, P. Selzer, J. Med. Chem. 43, 3714 (2000)CrossRef
    60.D. Greenwood, R.C.B. Slack, J.F. Peutherer, Medical Microbiology, 14th edn. (ELBS, London, 1992)
    61.M. Burits, F. Bucar, Phytother. Res. 14, 323 (2000)CrossRef
    62.C.A. Lipinski, L. Lombardo, B.W. Dominy, P.J. Feeney, Adv. Drug Deliv. Rev. 46, 3 (2001)CrossRef
    63.Molinspiration Chemoinformatics Brastislava, Slovak Republic. http://​www.​molinspiration.​com/​cgi-bin/​properties (2014)
    64.Y. Zhao, M.H. Abraham, J. Lee, A. Hersey, N.C. Luscombe, G. Beck, B. Sherborne, I. Cooper, Pharm. Res. 19, 1446 (2002)CrossRef
    65.Drug-likeness and molecular property prediction, available from: http://​www.​molsoft.​com/​mprop/​
  • 作者单位:Mubarak H. Shaikh (1)
    Dnyaneshwar D. Subhedar (1)
    Firoz A. Kalam Khan (2)
    Jaiprakash N. Sangshetti (2)
    Bapurao B. Shingate (1)

    1. Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad, 431 004, India
    2. Department of Pharmaceutical Chemistry, Y. B. Chavan College of Pharmacy, Dr. Rafiq Zakaria Campus, Aurangabad, 431 001, India
  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Chemistry
    Catalysis
    Physical Chemistry
    Inorganic Chemistry
  • 出版者:Springer Netherlands
  • ISSN:1568-5675
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