: Benzoylated phenyl α - and β - 2-thio-D-fructofuranosides were synthesthed and firstly used as donors in coupling with sucrose acceptor. a-Fructohanoside was stereospecifically synthesized by employing NIS(N - iod...: Benzoylated phenyl α - and β - 2-thio-D-fructofuranosides were synthesthed and firstly used as donors in coupling with sucrose acceptor. a-Fructohanoside was stereospecifically synthesized by employing NIS(N - iodosuccinimide)/AgOTf as catalysts. The structure of all products was confirmed by 13C-NMR or 1H-NMR spectrum展开更多
This work is describing a thionization method for glycosyl urea and carbamide of sugars by using the Lawesson’s reagent. It is proposed the method based on the interaction of glycosyl urea and carbamide of sugars wit...This work is describing a thionization method for glycosyl urea and carbamide of sugars by using the Lawesson’s reagent. It is proposed the method based on the interaction of glycosyl urea and carbamide of sugars with the Lawessons reagent at a 1:1 ratio in the presence of a pyridine. As a result, sulfur-containing derivatives of sugar carbamides are obtained with the help of Lawesson’s reagent. Obtained experimental data are indicating the developed new method for thionization of sugar carbamides, which opens up broad possibilities for synthesis of various carbohydrate derivatives of thiourea. Significance of this work is that, thiourea derivatives are promising bactericidal, fungicidal and anti-inflammatory drugs. Therefore, the preparation of thiourea derivatives and the study of their properties remain topical tasks in the field of chemistry.展开更多
文摘: Benzoylated phenyl α - and β - 2-thio-D-fructofuranosides were synthesthed and firstly used as donors in coupling with sucrose acceptor. a-Fructohanoside was stereospecifically synthesized by employing NIS(N - iodosuccinimide)/AgOTf as catalysts. The structure of all products was confirmed by 13C-NMR or 1H-NMR spectrum
文摘This work is describing a thionization method for glycosyl urea and carbamide of sugars by using the Lawesson’s reagent. It is proposed the method based on the interaction of glycosyl urea and carbamide of sugars with the Lawessons reagent at a 1:1 ratio in the presence of a pyridine. As a result, sulfur-containing derivatives of sugar carbamides are obtained with the help of Lawesson’s reagent. Obtained experimental data are indicating the developed new method for thionization of sugar carbamides, which opens up broad possibilities for synthesis of various carbohydrate derivatives of thiourea. Significance of this work is that, thiourea derivatives are promising bactericidal, fungicidal and anti-inflammatory drugs. Therefore, the preparation of thiourea derivatives and the study of their properties remain topical tasks in the field of chemistry.
