714250-66-5Relevant academic research and scientific papers
Synthesis of 2-substituted pyrimidines and benzoxazoles via a visible-light-driven organocatalytic aerobic oxidation: Enhancement of the reaction rate and selectivity by a base
Wang, Lin,Ma, Zhi-Gang,Wei, Xiao-Jing,Meng, Qing-Yuan,Yang, Deng-Tao,Du, Shao-Fu,Chen, Zi-Fei,Wu, Li-Zhu,Liu, Qiang
supporting information, p. 3752 - 3757 (2014/08/05)
An efficient visible-light-driven photocatalytic oxidation of various 2-substituted dihydropyrimidines and phenolic imines has been achieved using an organic photocatalyst eosin Y bis(tetrabutyl ammonium salt) (TBA-eosin Y) and inexpensive oxidant molecular oxygen. With the aid of a base, significantly enhanced photoinduced electron transfer from substrates dihydropyrimidines or phenolic imines to the excited state of TBA-eosin Y has enabled the aerobic oxidation to yield 2-(methylthio)pyrimidines or 2-arylbenzoxazoles selectively. This journal is the Partner Organisations 2014.
Synthesis of 2,3-Dihydro-1,3,4-thiadiazole, Thiazole, and Triazolo[4,3-a]pyrimidine Derivatives from Ethyl Benzoylacetate
Rateb, Nora M.,Abdelhamid, Abdou O.
, p. 107 - 113 (2007/10/03)
Thiophene and thiazole derivatives can be obtained from potassium salt of ethyl 3-oxo-3-phenyl-2-[(phenylamino)thioxomethyl]propanoate and ethyl chloroacetate in N,N-dimethylformamide solution under different conditions. 2,3-Dihydro-1,3,4-thiadiazoles and triazolo[4,3-a]pyrimidine were obtained from reaction of hydrazonoyl halides with each of thioanilide and pyrimidine-2-thione, respectively. Structures of the newly synthesized compounds were elucidated on the basis of elemental analysis, spectral data, and alternative synthesis route whenever possible.
