Search Results - "Kolomoets, Oleksandra S"
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1
Preparation and biological properties of 2-thio-containing pyrimidines and their condensed analogs
Published in Chemistry of heterocyclic compounds (New York, N.Y. 1965) (01-03-2017)“…The known methods for synthesis of thioxopyrimidines and their condensed analogs with exocyclic sulfur atom are summarized and discussed. The most popular…”
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2
Synthesis and Hypolipidemic Activity of New 6,6‐Disubstituted 3‐R‐6,7‐Dihydro‐2H‐[1,2,4]triazino[2,3‐c]quinazolin‐2‐Ones
Published in Journal of heterocyclic chemistry (01-01-2018)“…Presented article describes the synthesis and hypolipidemic activity of previously unknown 6,6‐disubstituted…”
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3
Synthesis, Modification, and Anticonvulsant Activity of 3′‐R 1 ‐Spiro[indoline‐3,6′‐[1,2,4]triazino[2,3 ‐c ]quinazolin]‐2,2′(7′ H )‐diones Derivatives
Published in Journal of heterocyclic chemistry (01-05-2019)“…Previously unknown 3′‐R 1 ‐5‐R 2 ‐spiro[indoline‐3,6′‐[1,2,4]triazino[2,3‐ c ]quinazoline]‐2,2′‐(7′ H )‐diones and their N‐substituted analogues were obtained…”
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4
Synthesis, Modification, and Anticonvulsant Activity of 3′‐R1‐Spiro[indoline‐3,6′‐[1,2,4]triazino[2,3‐c]quinazolin]‐2,2′(7′H)‐diones Derivatives
Published in Journal of heterocyclic chemistry (01-05-2019)“…Previously unknown 3′‐R1‐5‐R2‐spiro[indoline‐3,6′‐[1,2,4]triazino[2,3‐c]quinazoline]‐2,2′‐(7′H)‐diones and their N‐substituted analogues were obtained via…”
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5
Synthesis, Modification, and Anticonvulsant Activity of 3′‐R1‐Spirotriazinoquinazolin]‐2,2′(7′H)‐diones Derivatives
Published in Journal of heterocyclic chemistry (01-05-2019)“…Previously unknown 3′‐R1‐5‐R2‐spiro[indoline‐3,6′‐[1,2,4]triazino[2,3‐c]quinazoline]‐2,2′‐(7′H)‐diones and their N‐substituted analogues were obtained via…”
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6
Synthesis and Hypolipidemic Activity of New 6,6‐Disubstituted 3‐R‐6,7‐Dihydro‐2 H ‐[1,2,4]triazino[2,3‐ c ]quinazolin‐2‐Ones
Published in Journal of heterocyclic chemistry (01-01-2018)“…Presented article describes the synthesis and hypolipidemic activity of previously unknown 6,6‐disubstituted 3‐R‐6,7‐dihydro‐2 H ‐[1,2,4]triazino[2,3‐ c…”
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