The cyclizaion reactions of Lawesson's reagent(LR) with the substrates containing two functional groups such as hydroxy groups,amino groups, has been applied to prepare the O-P-O,N-P-N type 5-membered and 6-member...The cyclizaion reactions of Lawesson's reagent(LR) with the substrates containing two functional groups such as hydroxy groups,amino groups, has been applied to prepare the O-P-O,N-P-N type 5-membered and 6-membered phosphorus heterocycles.The heterocyclizaional possibility of LR with bifunctional compounds was also discussed.展开更多
The title compound, C31H30N3OPS3, crystallizes in monoclinic system, space group P21/n,with a = 11.839(7), b = 8.975(5), c = 29.15(2)? b = 100.07(1), V = 3049(3)?, Z = 4, Dc = 1.280g/cm3, Mr = 587.73, F(000) = 1232, m...The title compound, C31H30N3OPS3, crystallizes in monoclinic system, space group P21/n,with a = 11.839(7), b = 8.975(5), c = 29.15(2)? b = 100.07(1), V = 3049(3)?, Z = 4, Dc = 1.280g/cm3, Mr = 587.73, F(000) = 1232, m = 0.324mm-1, the final R = 0.0434 and wR = 0.1140 for 4787 observed reflections with I >2s(I). The title compound is a five-membered heterocycle containing a phosphorus, two nitrogen and two carbon atoms.The analysis result shows that the five-membered ring is nearly coplanar. The P(1)N(1) bond length(1.685? indicates the existence of pd?bond between N(1) and P(1) atoms of the title compound.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The cyclizaion reactions of Lawesson's reagent(LR) with the substrates containing two functional groups such as hydroxy groups,amino groups, has been applied to prepare the O-P-O,N-P-N type 5-membered and 6-membered phosphorus heterocycles.The heterocyclizaional possibility of LR with bifunctional compounds was also discussed.
基金This project was supported by Foundation for University Key Teacher by the Ministry of Education
文摘The title compound, C31H30N3OPS3, crystallizes in monoclinic system, space group P21/n,with a = 11.839(7), b = 8.975(5), c = 29.15(2)? b = 100.07(1), V = 3049(3)?, Z = 4, Dc = 1.280g/cm3, Mr = 587.73, F(000) = 1232, m = 0.324mm-1, the final R = 0.0434 and wR = 0.1140 for 4787 observed reflections with I >2s(I). The title compound is a five-membered heterocycle containing a phosphorus, two nitrogen and two carbon atoms.The analysis result shows that the five-membered ring is nearly coplanar. The P(1)N(1) bond length(1.685? indicates the existence of pd?bond between N(1) and P(1) atoms of the title compound.
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.
