[1]JournalofHeterocyclicChemistry,1992,vol.29,#5,p.1369-1370
[2]Patent:US5278175,1994,A,
[1]JournalofMedicinalChemistry,2014,vol.57,#6,p.2429-2439
[1]Patent:US5652246,1997,A,
[1]Heterocycles,2000,vol.53,#3,p.549-552
[1]CroaticaChemicaActa,2016,vol.89,#4,
[1]CurrentPatentAssignee:TAKASAGOINTERNATIONALCORPORATION-WO2004/74255,2004,A2Locationinpatent:Page74-75
[2]CurrentPatentAssignee:TAKASAGOINTERNATIONALCORPORATION-WO2004/74255,2004,A2Locationinpatent:Page82-83
[3]CurrentPatentAssignee:TAKASAGOINTERNATIONALCORPORATION-WO2004/74255,2004,A2Locationinpatent:Page83
[4]CurrentPatentAssignee:TAKASAGOINTERNATIONALCORPORATION-WO2004/74255,2004,A2Locationinpatent:Page82
[5]CurrentPatentAssignee:TAKASAGOINTERNATIONALCORPORATION-WO2004/74255,2004,A2Locationinpatent:Page81-82
[6]Bradbury;Allott;Dennis;Fisher;Major;Masek;Oldham;Pearce;Rankine;Revill;Roberts;Russell[JournalofMedicinalChemistry,1992,vol.35,#22,p.4027-4038]
[1]Synthesis,1990,p.382-386
[1]JournalofHeterocyclicChemistry,1992,vol.29,p.1369-1370
[2]Patent:US5278175,1994,A
[1]TetrahedronLetters,1986,vol.27,p.2657-2660
[2]TetrahedronLetters,1989,vol.30,p.2245-2246
[3]ChemistryLetters,1987,p.679-682
[4]BulletinoftheChemicalSocietyofJapan,1989,vol.62,p.875-879
[5]ChemistryLetters,1987,p.1267-1270
[6]ChemistryLetters,1987,p.679-682
[7]BulletinoftheChemicalSocietyofJapan,1994,vol.67,p.2473-2477
[8]BulletinoftheChemicalSocietyofJapan,1983,vol.56,p.1414-1419
[9]TetrahedronLetters,1997,vol.38,p.6603-6606
[10]TetrahedronLetters,1990,vol.31,p.267-270
[11]TetrahedronLetters,1989,vol.30,p.2245-2246
[12]ChemistryLetters,1987,p.1267-1270
[13]TetrahedronLetters,1997,vol.38,p.6603-6606
[14]ChemistryLetters,1998,p.1257-1258
[15]JournalofOrganicChemistry,2000,vol.65,p.2586-2587
[16]JournaloftheAmericanChemicalSociety,2001,vol.123,p.1547-1555
[17]BulletinoftheChemicalSocietyofJapan,2002,vol.75,p.355-363
[18]BulletinoftheChemicalSocietyofJapan,2002,vol.75,p.355-363
[19]AngewandteChemie-InternationalEdition,2004,vol.43,p.5066-5069
[20]AdvancedSynthesisandCatalysis,2005,vol.347,p.1978-1986
[21]AdvancedSynthesisandCatalysis,2006,vol.348,p.1157-1160
[22]TetrahedronLetters,2006,vol.47,p.4033-4035
[23]TetrahedronLetters,1985,vol.26,p.4213-4216
[24]AdvancedSynthesisandCatalysis,2003,vol.345,p.160-164
[25]Patent:US6939981,2005,B1.Locationinpatent:Page/Pagecolumn16-17
[26]AdvancedSynthesisandCatalysis,2009,vol.351,p.725-732
[27]AdvancedSynthesisandCatalysis,2013,vol.355,p.209-219
[28]AdvancedSynthesisandCatalysis,2013,vol.355,p.209-219
[29]EuropeanJournalofInorganicChemistry,2017,vol.2017,p.2762-2773
[1]TetrahedronAsymmetry,1991,vol.2,p.569-592
[2]TetrahedronAsymmetry,1994,vol.5,p.675-690
[3]JournalofOrganicChemistry,2004,vol.69,p.7577-7581
[4]ChemicalCommunications,2019,vol.56,p.157-160
[5]EuropeanJournalofOrganicChemistry,2014,vol.2014,p.323-330
[6]EuropeanJournalofOrganicChemistry,2014,vol.2014,p.323-330
[7]Synlett,2011,p.191-194
[8]JournaloftheAmericanChemicalSociety,1987,vol.109,p.5856-5858
[9]TetrahedronLetters,1995,vol.36,p.4801-4804
[10]JournaloftheAmericanChemicalSociety,1995,vol.117,p.4423-4424
[11]Tetrahedron,2001,vol.57,p.2563-2568
[12]JournaloftheAmericanChemicalSociety,2001,vol.123,p.1547-1555
[13]Patent:US6359165,2002,B1.Locationinpatent:Pagecolumn13
[14]Patent:US6939981,2005,B1.Locationinpatent:Page/Pagecolumn14
[15]Patent:US2008/255355,2008,A1.Locationinpatent:Page/Pagecolumn8-9
[16]Patent:US2005/250951,2005,A1.Locationinpatent:Page/Pagecolumn12
[17]Patent:US2005/250951,2005,A1.Locationinpatent:Page/Pagecolumn13
[18]Patent:US2005/250951,2005,A1.Locationinpatent:Page/Pagecolumn12
[19]AdvancedSynthesisandCatalysis,2013,vol.355,p.209-219
[20]Patent:US9250238,2016,B2.Locationinpatent:Page/Pagecolumn106;107;108
[21]CuihuaXuebao/ChineseJournalofCatalysis,2017,vol.38,p.890-897
Title: 2-Ethyl 4-methyl 5-ethyl-3-methyl-1H-pyrrole-2,4-dicarboxyl-ate.
Journal: Acta crystallographica. Section E, Structure reports online 20120201
Title: Dimethyl 3,5-diethyl-1H-pyrrole-2,4-dicarboxyl-ate.
Journal: Acta crystallographica. Section E, Structure reports online 20110801
Title: Studies on the synthesis and biological activitiy of 6-ethyl-4-aryl-5-methoxycarbonyl-3,4-dihydropyrimidin-2(1H)-ones.
Journal: Arzneimittel-Forschung 20070101
Title: Synthesis of 4-aryl-3,4-dihydropyrimidin-2(1H)-thione derivatives as potential calcium channel blockers.
Journal: Bioorganic & medicinal chemistry 20061215