1-Phenyl-1,3-butandione benzidine diketoimine 2a （C32H28N2O2, Mr = 472.56） was synthesized in high yield by the reaction of 1-phenyl-1,3-butandione with benzidine in absolute ethanol, and determined by X-ray structu...1-Phenyl-1,3-butandione benzidine diketoimine 2a （C32H28N2O2, Mr = 472.56） was synthesized in high yield by the reaction of 1-phenyl-1,3-butandione with benzidine in absolute ethanol, and determined by X-ray structure analysis. It crystallizes in the orthorhombic system, space group P21/c with a = 7.9839（16）, b = 12.910（3）, c = 12.358（3）A, α = 90.00, β= 93.71（3）,γ = 90.00°, V = 1271.1（4） A3, Z = 2, Dc = 1.235 g/cm^3,/1 = 0.077 mm^-1, F（000） = 500, the final R = 0.0717 and wR = 0.1187. It presents a linear centrosymmetric framework constituted by a linkage of benzidine as a bridge and two terminal 1-phenyl-1,3-butanedione moieties.展开更多
Herein, a facile synthesis of valuable pyrido[1,2-a]pyrimidine-4-thiones is reported via novel thiocarbonylation of C(sp^(3))-H bonds with carbon disulfide(CS_(2)). This reaction features easy availability of substrat...Herein, a facile synthesis of valuable pyrido[1,2-a]pyrimidine-4-thiones is reported via novel thiocarbonylation of C(sp^(3))-H bonds with carbon disulfide(CS_(2)). This reaction features easy availability of substrates,good functional group tolerance, high yields, facile scalability and atom economy. Mechanistic investigations indicate that sulfate anion and sulfuric anhydride anion might be involved in this reaction.展开更多
文摘1-Phenyl-1,3-butandione benzidine diketoimine 2a （C32H28N2O2, Mr = 472.56） was synthesized in high yield by the reaction of 1-phenyl-1,3-butandione with benzidine in absolute ethanol, and determined by X-ray structure analysis. It crystallizes in the orthorhombic system, space group P21/c with a = 7.9839（16）, b = 12.910（3）, c = 12.358（3）A, α = 90.00, β= 93.71（3）,γ = 90.00°, V = 1271.1（4） A3, Z = 2, Dc = 1.235 g/cm^3,/1 = 0.077 mm^-1, F（000） = 500, the final R = 0.0717 and wR = 0.1187. It presents a linear centrosymmetric framework constituted by a linkage of benzidine as a bridge and two terminal 1-phenyl-1,3-butanedione moieties.
基金the National Natural Science Foundation of China (No. 21822108)Sichuan Science and Technology Program (Nos.20CXTD0112, 2020YJ0491)+1 种基金National Key Research and Development Program of China (No. 2018YFC1602101)the Fundamental Research Funds for the Central Universities。
文摘Herein, a facile synthesis of valuable pyrido[1,2-a]pyrimidine-4-thiones is reported via novel thiocarbonylation of C(sp^(3))-H bonds with carbon disulfide(CS_(2)). This reaction features easy availability of substrates,good functional group tolerance, high yields, facile scalability and atom economy. Mechanistic investigations indicate that sulfate anion and sulfuric anhydride anion might be involved in this reaction.
