1,2-benzoxathiin-4(3h)-one 2,2-dioxide – an underinvestigated building block with a high synthetic and pharmacological potential: synthesis, chemical properties, biological activit...

за авторством H. V. Hryhoriv, D. A. Lega, L. A. Shemchuk
Опубліковано 2021

The study of the three-component interaction between 1-ethyl-1N-2,1-benzothiazin-4(3N)-one 2,2-dioxide, heterylcarbaldehydes and active methylene nitriles

за авторством D. A. Lega, V. P. Chernykh, L. A. Shemchuk
Опубліковано 2016

Domino-reactions of 1,2-benzoxathiin-4(3H)-one 2,2-dioxide, hetarenecarbaldehydes and active methylene nitriles in the construction of new 2-amino-4H-pyrans and the study of their...

за авторством G. V. Grygoriv, D. A. Lega, V. P. Chernykh, T. P. Osolodchenko, L. A. Shemchuk
Опубліковано 2018

The use of aliphatic aldehydes in the synthesis of new pyran annulated derivatives of 1H-2,1-benzothiazin-4-one 2,2-dioxide via domino-type interactions. The antimicrobial activity...

за авторством D. A. Lega, N. I. Filimonova, O. G. Geyderikh, V. P. Chernykh, L. A. Shemchuk
Опубліковано 2016

The synthesis and antiviral activity against yellow fewer virus of 2-(4,6-di(pyrrolidin-1-yl)-1,3,5-triazin-2-yl)-N-(alkyl, aryl)hydrazine-1-carbothioamides

за авторством O. V. Moskalenko, O. I. Barchina, S. A. Tsyhankov, D. A. Lega, Yu. A. Fedchenkova, A. M. Demchenko
Опубліковано 2021

The synthesis, anti-inflammatory, analgesic and antimicrobial activities of ethyl 2-amino-4-alkyl-4,6-dihydropyrano(3,2-c)(2,1)benzothiazin-3-carboxylate 5,5-dioxides and triethyla...

за авторством D. A. Lega, N. I. Filimonova, I. A. Zupanets, S. K. Shebeko, V. P. Chernykh, L. A. Shemchuk
Опубліковано 2016

Spiro|benzo|e|pyrano|3,2-c||1,2|oxathiin-4,3'-indolil|-3-carbonitrile 5,5-dioxides: synthesis and the biological activity study

за авторством G. V. Grygoriv, D. A. Lega, I. A. Zupanets, S. K. Shebeko, S. M. Zimin, I. L. Starchikova, L. A. Shemchuk
Опубліковано 2019

Multi-faceted commercially sourced pd-supported reduction: a view from practical experience

за авторством V. V. Burianov, D. A. Lega, V. G. Makhankova, Yu. M. Volovenko, S. V. Kolotilov, D. M. Volochnyuk, S. V. Ryabukhin
Опубліковано 2022