Results 171 to 180 of about 4,465 (196)
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Monothio- and dithiophosphonoacetylphenothiazines and phenoxazines
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 19711. The previously unknown 10-[(O,O-dialkylphosphonothio)acetyl]phenothiazines (alkyl: ethyl, propyl, i-propyl, butyl, i-butyl), 10-methyl(ethyl)-3-[(O,O-diethylthionophosphonothlo)acetamido]phenothiazines, [(O,O-diethyldithiophosphono)acetyl]phenothiazine, 10-(O,O-diethylphosphonothioacetyl)phenoxazine, 10-[(O,O-dialkyldithiophosphono) acetyl ...
D. Kh. Yarmukhametova +3 more
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Antiviral activity spectrum of phenoxazine nucleoside derivatives
Antiviral Research, 2019The phenoxazine scaffold is widely used to stabilize nucleic acid duplexes, as a part of fluorescent probes for the study of nucleic acid structure, recognition, and metabolism, etc. Here we present the synthesis of phenoxazine-based nucleoside derivatives and their antiviral activity against a panel of structurally diverse viruses: enveloped DNA ...
Liubov I. Kozlovskaya +11 more
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Investigation of the chemistry of phenoxazines
Chemistry of Heterocyclic Compounds, 1972Depending on the position of the annelated benzene ring, benzophenoxazinones add thiophenols in the benzenoid, quinonoid, or both parts of the molecule to give mono- or diarylmercapto derivatives. A substituent in the benzenoid portion of the molecule hinders polarographic reduction and shifts the visible absorption band bathochromically, while a ...
G. B. Afanas'eva +5 more
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THE SYNTHESIS OF 10-SUBSTITUTED PHENOXAZINES
Canadian Journal of Chemistry, 1960not available
Gerassimos Frangatos +2 more
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Chemischer Informationsdienst. Organische Chemie, 1970
AbstractMethylierung von Imidazo(4,5,1‐kl)phenoxazin (I) mit dem aus Dimethylsulfoxid und Methyljodid erhältlichen Trimethylsulfoxoniumjodid (II) in Dimethlysulfoxid bei 105°C unter Stickstoff liefert in 82%iger Ausbeute 2‐Methyl‐1 ,2‐dihydroimidazo(4,5,1‐kl)phenoxazin‐1‐on (II), das auch aus 1,2‐Dihydroimidazo(4,5 ,1‐kl)phenoxazin‐1‐on (IV) mit ...
H. SHIRAI, T. HAYAZAKI
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AbstractMethylierung von Imidazo(4,5,1‐kl)phenoxazin (I) mit dem aus Dimethylsulfoxid und Methyljodid erhältlichen Trimethylsulfoxoniumjodid (II) in Dimethlysulfoxid bei 105°C unter Stickstoff liefert in 82%iger Ausbeute 2‐Methyl‐1 ,2‐dihydroimidazo(4,5,1‐kl)phenoxazin‐1‐on (II), das auch aus 1,2‐Dihydroimidazo(4,5 ,1‐kl)phenoxazin‐1‐on (IV) mit ...
H. SHIRAI, T. HAYAZAKI
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Tricyanovinylation of phenoxazine and phenothiazine
Chemistry of Heterocyclic Compounds, 1985In the reaction of tricyanoethylene (TCE) with phenoxazine in DMF at 100 ° C, in addition to the principal reaction product —viz., 3-(tricyanovinyl) phenoxazine — 3-dicyanomethylene-3H-phenoxazine and 3-phenoxazinyl-3-(3H-phenoxazinylene)-cyanomethane are formed in small amounts.
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Nitrogen Substituted Phenoxazines
Journal of Medicinal Chemistry, 1963A E, GAL, S, AVAKIAN
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