[1]AmericanChemicalJournal,1896,vol.18,p.163,165
[2]YakugakuZasshi,1949,vol.69,p.417
[3]Chem.Abstr.,1950,p.1924
[4]Patent:WO2005/34885,2005,A1,.Locationinpatent:Page/Pagecolumn36
[1]AmericanChemicalJournal,1896,vol.18,p.163,165
[1]Patent:CN105801455,2016,A,.Locationinpatent:Paragraph0048
[2]Patent:US2004/58977,2004,A1,.Locationinpatent:Page/Pagecolumn8;14
[3]AmericanChemicalJournal,1885,vol.7,p.147
[4]JustusLiebigsAnnalenderChemie,1875,vol.178,p.284
[5]JournaloftheChemicalSociety,1951,p.1877,1880
[6]BollettinoChimicoFarmaceutico,1956,vol.95,p.287,290
[7]Rep.Gov.chem.ind.Res.Inst.Tokyo,1950,vol.45,p.295,297
[8]Chem.Abstr.,1952,p.4269
[9]BioorganicandMedicinalChemistry,2014,vol.22,#6,p.1873-1882
[10]Patent:CN105693565,2016,A,.Locationinpatent:Paragraph0044;0045;0046
[11]BioorganicandMedicinalChemistry,2017,vol.25,#3,p.1286-1293
[1]JournalofMedicinalChemistry,1988,vol.31,#9,p.1762-1767
[2]VerslagvandeGewoneVergaderingvandeAfdelingNatuurkunde,KoninklijkeNederlandseAkademievanWetenschappen,vol.32,p.15
[3]Chem.Zentralbl.,1923,vol.94,#III,p.302
[4]JournalofOrganicChemistry,1968,vol.33,#9,p.3610-3618
[5]Patent:US5935990,1999,A,
[1]Synthesis,2000,#5,p.646-650
[2]JournalofOrganicChemistry,1968,vol.33,#9,p.3610-3618
[1]JournaloftheChemicalSociety,1951,p.1877,1880
[2]MagneticResonanceinChemistry,1989,vol.27,p.585-591
[1]JournaloftheAmericanChemicalSociety,2006,vol.128,p.3273-3280
[2]JournalofMedicinalChemistry,2010,vol.53,p.4555-4559
[3]EuropeanJournalofMedicinalChemistry,2018,vol.156,p.430-443
[4]Patent:CN110903262,2020,A.Locationinpatent:Paragraph0059-0063
[5]Patent:WO2009/115515,2009,A1.Locationinpatent:Page/Pagecolumn26
[6]AdvancedSynthesisandCatalysis,2020,vol.362,p.561-571
[7]BollettinoChimicoFarmaceutico,1997,vol.136,p.244-249
[8]Patent:WO2007/23186,2007,A1.Locationinpatent:Page/Pagecolumn49
[9]Tetrahedron,1993,vol.49,p.11329-11340
[10],1949,vol.39,p.109,112,113
[11]KagakuKenkyushoHokoku,1950,vol.26,p.301,302
[12]JournalofMedicinalChemistry,2005,vol.48,p.2121-2125
[13]BioorganicandMedicinalChemistry,2009,vol.17,p.3028-3036
[14]BioorganicandMedicinalChemistry,2014,vol.22,p.1873-1882
[15]ACSMedicinalChemistryLetters,2017,vol.8,p.792-796
[16]EuropeanJournalofMedicinalChemistry,2018,vol.157,p.28-36
[17]BioorganicandMedicinalChemistry,2019,vol.27,p.1087-1098
[18]EuropeanJournalofMedicinalChemistry,2020,vol.193
[1]JournalofMedicinalChemistry,1988,vol.31,p.1762-1767
[2]VerslagvandeGewoneVergaderingvandeAfdelingNatuurkunde,KoninklijkeNederlandseAkademievanWetenschappen,vol.32,p.15 ChemischesZentralblatt,1923,vol.94,p.302
[3]JournalofOrganicChemistry,1968,vol.33,p.3610-3618
[4]Patent:US5935990,1999,A
[1]Patent:CN105801455,2016,A.Locationinpatent:Paragraph0048
[2]Patent:US2004/58977,2004,A1.Locationinpatent:Page/Pagecolumn8;14
[3]AdvancedSynthesisandCatalysis,2020,vol.362,p.561-571
[4]AmericanChemicalJournal,1885,vol.7,p.147
[5]JustusLiebigsAnnalenderChemie,1875,vol.178,p.284
[6]JournaloftheChemicalSociety,1951,p.1877,1880
[7]BioorganicandMedicinalChemistry,2014,vol.22,p.1873-1882
[8]Patent:CN105693565,2016,A.Locationinpatent:Paragraph0044;0045;0046
[9]BioorganicandMedicinalChemistry,2017,vol.25,p.1286-1293
[10]EuropeanJournalofMedicinalChemistry,2020,vol.193
[1]Patent:JP5676853,2015,B2.Locationinpatent:Paragraph0072-0074
[2]JournaloftheAmericanChemicalSociety,1994,vol.116,p.5057-5062
[3]Chemistry-AnAsianJournal,2012,vol.7,p.1567-1571
[4]Chemistry-AEuropeanJournal,2004,vol.10,p.2375-2385
[5]JournalofMedicinalChemistry,2015,vol.58,p.4039-4045
[6]ChemicalCommunications,2015,vol.51,p.17265-17268
[7]AngewandteChemie-InternationalEdition,2005,vol.44,p.5480-5483
[8]BioorganicandMedicinalChemistryLetters,1996,vol.6,p.559-564
[9]AngewandteChemie-InternationalEdition,2014,vol.53,p.4231-4235 Angew.Chem.,2014,vol.126,p.4315-4320,6
[10]JournaloftheAmericanChemicalSociety,2015,vol.137,p.7286-7289
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