Novel 3,3-disubstituted oxindole derivatives. Synthesis and evaluation of the anti-proliferative activity
Tài liệu tham khảo
Lin, 2003, Angew Chem Int Ed, 42, 36, 10.1002/anie.200390048
Marti, 2003, Eur J Org Chem, 2003, 2209, 10.1002/ejoc.200300050
Singh, 2012, Chem Rev, 112, 6104, 10.1021/cr300135y
Song, 2016, Eur J Med Chem, 124, 809, 10.1016/j.ejmech.2016.09.005
Cao, 2018, Acc Chem Res, 51, 1443, 10.1021/acs.accounts.8b00097
Cui, 1996, Tetrahedron, 52, 12651, 10.1016/0040-4020(96)00737-5
Galliford, 2007, Angew Chem Int Ed, 46, 8748, 10.1002/anie.200701342
Zhao, 2013, J Med Chem, 56, 5553, 10.1021/jm4005708
Yu, 2015, Eur J Med Chem, 97, 673, 10.1016/j.ejmech.2014.06.056
Teng, 2006, Molecules, 11, 700, 10.3390/11090700
Zhou, 2010, Adv Synth Catal, 352, 1381, 10.1002/adsc.201000161
Klein, 2011, Eur. J. Org. Chem., 2011, 6821, 10.1002/ejoc.201100836
Hong, 2013, Adv Synth Catal, 355, 1023, 10.1002/adsc.201200808
Moyano, 2013, Elsevier Ed., 71
Tak, 2018, Eur. J Org Chem, 2018, 5678, 10.1002/ejoc.201801002
Sato, 2009, J Org Chem, 74, 7522, 10.1021/jo901352u
Tokunaga, 2001, J Med Chem, 44, 4641, 10.1021/jm0103763
Bernard, 2005, Br J Pharmacol, 144, 1037, 10.1038/sj.bjp.0706103
Shimazaki, 2006, Eur J Pharmacol, 543, 63, 10.1016/j.ejphar.2006.06.032
Decaux, 2008, The Lancet, 371, 1624, 10.1016/S0140-6736(08)60695-9
Ghosh, 2006, Bioorg Med Chem Lett, 16, 1869, 10.1016/j.bmcl.2006.01.011
Shanmugam, 2007, Org Lett, 9, 4095, 10.1021/ol701533d
Kouznetsov, 2008, Tetrahedron Lett, 49, 5855, 10.1016/j.tetlet.2008.07.096
Rainoldi, 2018, RSC Adv, 8, 34903, 10.1039/C8RA08165D
Bui, 2009, J Org Chem, 74, 8935, 10.1021/jo902039a
Cheng, 2009, Org Lett, 11, 3874, 10.1021/ol901405r
Lesma, 2009, J Org Chem, 74, 4537, 10.1021/jo900623c
Qian, 2009, Chem Commun, 6753, 10.1039/b915257a
Bui, 2010, Org Lett, 12, 5696, 10.1021/ol102493q
Mouri, 2010, J Am Chem Soc, 132, 1255, 10.1021/ja908906n
Yang, 2010, Chem Eur J, 16, 6632, 10.1002/chem.201000126
Beccalli, 2001, Tetrahedron, 57, 4787, 10.1016/S0040-4020(01)00404-5
Beccalli, 2003, Tetrahedron, 59, 4615, 10.1016/S0040-4020(03)00627-6
Christodoulou, 2018, ChemistrySelect, 3, 4361, 10.1002/slct.201800568
Beccalli, 2010, J Org Chem, 75, 6923, 10.1021/jo101501u
Broggini, 2013, Adv Synth Catal, 355, 1640, 10.1002/adsc.201300104
Beccalli, 1992, Tetrahedron, 48, 5359, 10.1016/S0040-4020(01)89032-3
Mazza, 2016, Eur J Med Chem, 124, 326, 10.1016/j.ejmech.2016.08.045
Christodoulou, 2016, Eur J Med Chem, 118, 79, 10.1016/j.ejmech.2016.03.090
Gabriele, 2017, Arkivoc, 235
Christodoulou, 2015, ChemPlusChem, 80, 938, 10.1002/cplu.201402435
Rimoldi, 2018, Biomed Pharmacother, 108, 111, 10.1016/j.biopha.2018.09.040
Christodoulou, 2017, ChemMedChem, 12, 33, 10.1002/cmdc.201600474
Marucci, 2016, Eur J Org Chem, 2016, 2029, 10.1002/ejoc.201600130
Carlino, 2018, ChemMedChem, 13, 2627, 10.1002/cmdc.201800687
Quaglio, 2019, ACS Med Chem Lett, 10, 639, 10.1021/acsmedchemlett.8b00608
Facchetti, 2019, Eur J Inorg Chem, 2019, 3389, 10.1002/ejic.201900644
Ferri, 2011, Bioorg Med Chem, 19, 5291, 10.1016/j.bmc.2011.08.016
Ferri, 2008, Bioorg Med Chem, 16, 1691, 10.1016/j.bmc.2007.11.024