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Synthesis, spectroscopic structure identification, X-ray study and anticancer activities of new angularly fused quinobenzothiazines

Pluta K., Szmielew M., Suwińska K., Latocha M.

analysis was based on 1D and 2D NMR (NOESY, COSY, HSQC and HMBC) spectra which enabled to distinguish

Uncharged water-soluble amide derivatives of pillar[5]arene: synthesis and supramolecular self-assembly with tetrazole-containing polymers

Shurpik D.N., Nazarova A.A., Makhmutova L.I., Kizhnyaev V.N., Stoikov I.I.

, and HSQC NMR) allowed us to determine the spatial structure of the synthesized macrocycles. Aggregation

Synthesis, spectroscopic structure identification, X-ray study and anticancer activities of new angularly fused quinobenzothiazines

Pluta K., Szmielew M., Suwińska K., Latocha M.

analysis was based on 1D and 2D NMR (NOESY, COSY, HSQC and HMBC) spectra which enabled to distinguish

Двумерная ямр спектроскопия в качественном анализе биологически активных веществ на примере алкалоидов

Белов Константин Васильевич, Ходов Илья Анатольевич, Киселев Михаил Григорьевич

The double Smiles rearrangement in neutral conditions leading to one of 10-(nitropyridinyl)dipyridothiazine isomers

Morak-Młodawska B., Pluta K., Suwińska K., Jeleń M.

nitropyridinyldipyridothiazines. Two-dimensional 1H and 13C NMR experiments (COSY, ROESY, HSQC and HMBC) were used to reveal

CRYSTALLINE STRUCTURE AND HIRSHFELD SURFACE ANALYSIS OF 7-((6-HYDROXY-2,5,5,8A-TETRAMETHYL-1,4,4A,5,6,7,8,8A OCTAHYDRONAPHTHALEN-1-YL)METHOXY)-2H-CHROMEN-2-ONE ISOLATED FROM FERULA PERSICA ROOTS: A NEW ENANTIOMORPH AT 100K

Karimli E.G., Mamedov İ.G., Khrustalev V.N., Akkurt M., Khalilov A.N., Mamedov A.M., Kerimov Y.B., Ibadullayeva S.J., Aleskerova A.N.

used X-Ray, NMR 1H, 13C NMR, DEPT, COSY, HSQC, and HMBC methods. It has been previously mentioned about

The double Smiles rearrangement in neutral conditions leading to one of 10-(nitropyridinyl)dipyridothiazine isomers

Morak-Młodawska B., Pluta K., Suwińska K., Jeleń M.

nitropyridinyldipyridothiazines. Two-dimensional 1H and 13C NMR experiments (COSY, ROESY, HSQC and HMBC) were used to reveal

Evaluation of angularly condensed diquinothiazines as potential anticancer agents

Jeleń M., Pluta K., Latocha M., Morak-Młodawska B., Suwińska K., Kuśmierz D.

′,7′-e][1,4]thiazine with advanced two-dimensional 1 H and 13 C NMR techniques (COSY, ROESY, HSQC

Строение лемнана - пектинового полисахарида из ряски малой Lemna minor L.: Автореф. дис.... канд. хим. наук: 02.00.10

Головченко В.В. (Виктория Владимировна), Оводов Ю.С. (Научный руководитель), Оводова Р.Г. (Научный руководитель), Институт физиологии Коми научного центра Уральского отделения Российской академии наук.

CRYSTALLINE STRUCTURE AND HIRSHFELD SURFACE ANALYSIS OF 7-((6-HYDROXY-2,5,5,8A-TETRAMETHYL-1,4,4A,5,6,7,8,8A-OCTAHYDRONAPHTHALEN-1-YL)METHOXY)-2H-CHROMEN-2-ONE ISOLATED FROM FERULA PERSICA ROOTS: A NEW ENANTIOMORPH AT 100K

Karimli E.G., Mamedov İ.G., Khrustalev V.N., Akkurt M., Khalilov A.N., Mamedov A.M., Kerimov Y.B., Ibadullayeva S.J., Aleskerova A.N.

used X-Ray, NMR ¹H, ¹³C NMR, DEPT, COSY, HSQC, and HMBC methods. It has been

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