[1]JournaloftheChemicalSociety,1957,p.253,255
[1]ElectrochemistryCommunications,2016,vol.68,p.59-61
[2]Chemistry-AEuropeanJournal,2009,vol.15,p.3882-3888
[3]ChemistryofHeterocyclicCompounds,1997,vol.33,p.1301-1305
[4]JustusLiebigsAnnalenderChemie,1884,vol.224,p.45
[5]JustusLiebigsAnnalenderChemie,1884,vol.224,p.45
[6]BulletinoftheChemicalSocietyofJapan,1988,vol.61,p.1633-1640
[7]RussianJournalofGeneralChemistry,2019,vol.89,p.918-923 Zh.Obshch.Khim.,2019,vol.89,p.726-732,7
[8]RussianJournalofOrganicChemistry,2019,vol.55,p.938-943 Zh.Org.Khim.,2019,vol.55,p.1030-1037
[1]JournaloftheAmericanChemicalSociety,2015,vol.137,p.11718-11724
[2]JustusLiebigsAnnalenderChemie,1884,vol.224,p.45
[3]JustusLiebigsAnnalenderChemie,1884,vol.224,p.45
[4]JustusLiebigsAnnalenderChemie,1928,vol.463,p.208
[5]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1959,vol.79,p.967 Chem.Abstr.,1959,p.21947
[6]JournaloftheChemicalSociety,1954,p.4142,4144
[7]JournalofHeterocyclicChemistry,1985,vol.22,p.879-881
[8]Heterocycles,1998,vol.48,p.1663-1668
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