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Synthesis and some reactions of 5-carbmethoxymethylidene-4-oxo-1,3-thiazol-2-ylguanidine
Stolpovskaya N.V., Kruzhilin A.A., Shvetsova E.S., Shikhaliev K.S., Zubkov F.I., Van Quy D.
been proven by X-ray diffraction analysis. A series of new N-(5-R-1,3,5-triazinan-2-ylidene)-N-1,3
Nuclease biosynthesis and growth of Serratia marcescens in the presence of 2-(p-aminobenzenesulfonamide)-thiazole
Starshinova N., Filimonova M.
synthesis inhibition with 2-(p-aminobenzenesulfonamide) -thiazole. The addition of this sulfonamide to S
Nuclease biosynthesis and growth of Serratia marcescens in the presence of 2-(p-aminobenzenesulfonamide)-thiazole
Starshinova N., Filimonova M.
synthesis inhibition with 2-(p-aminobenzenesulfonamide) -thiazole. The addition of this sulfonamide to S
Multicomponent Synthesis of Thiazole, Selenazole, Pyrane, and Pyridine Derivatives, Initiated by the Knoevenagel Reaction
Dyachenko I.V., Dyachenko V.D., Dorovatovskii P.V., Khrustalev V.N., Nenaidenko V.G.
(2E,2′E)-3,3′-(Propane-1,3-diyl)bis[oxy(4,1-phenylene)]bis[2-(4-aryl-1,3-thiazol-2-yl
Nuclease biosynthesis and growth of Serratia marcescens in the presence of 2-(p-aminobenzenesulfonamide)-thiazole
Starshinova N., Filimonova M.
synthesis inhibition with 2-(p-aminobenzenesulfonamide) -thiazole. The addition of this sulfonamide to S
Nuclease biosynthesis and growth of Serratia marcescens in the presence of 2-(p-aminobenzenesulfonamide)-thiazole
Starshinova N., Filimonova M.
synthesis inhibition with 2-(p-aminobenzenesulfonamide) -thiazole. The addition of this sulfonamide to S
Crystal structures of ethyl {2-[4-(4-isopropylphenyl)thiazol-2-yl]phenyl}carbamate and ethyl {2-[4-(3-nitrophenyl)thiazol-2-yl]phenyl}carbamate
Sukhonosova E.V., Sokov S.A., Ostapenko G.I., Bunev A.S., Dorovatovskii P.V., Zubavichus Y.V., Khrustalev V.N.
The title compounds, C21H22N2O2S (I) and C18H15N3O4S (II), are structural analogs of the alkaloid
Multicomponent Synthesis of Derivatives of Thiazole, Selenazole, Pyrane and Pyridine, Initiated by the Reaction of Knoevenagel
Dyachenko I.V., Dyachenko V.D., Dorovatovskii P.V., Khrustalev V.N., Nenaidenko V.G.
'-[propane-1,3-diylbis(oxy)bis(4,1-phenylene)]bis[2-(4-(4-arylthiazol-2-yl))acrylonitriles], functionally
Additional cycle formation from 2-dialkoxyphosphonylmethylthiazole
Baimashev B., Polezhaeva N., Klimovitskii E.
ethylenes were produced, whereas employing α-halocarbonyls as partners resulted in pyrrolo[2.1b]thiazoles. 1
Synthesis and Properties of 3-Substituted 2H-Chromen-2-ones
Dyachenko I.V., Dyachenko V.D., Dorovatovsky P.V., Khrustalev V.N., Nenaidenko V.G.
-amino-3-sulfanylidenepropanoate, 3-amino-N-aryl-3-sulfanylidenepropanamides, and ethyl 2-(1,3-thiazol-2

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