1574320-87-8Relevant articles and documents
Visible-light-initiated catalyst-free oxidative cleavage of (Z)-triaryl-substituted alkenes containing pyridyl motif under ambient conditions
Chen, Hua,Fu, Haiyan,Ge, Yicen,Li, Ruixiang,Li, Shun,Li, Wenjing,Luo, Lihua,Xu, Jiaqi,Yuan, Maolin,Zheng, Xueli
, p. 3649 - 3655 (2021/06/06)
The catalyst-free oxidative cleavage of (Z)-triaryl-substituted alkenes bearing a pyridyl motif in ambient air under the irradiation of blue LEDs at room temperature has been developed. The reaction was facile and scalable, and proceeded with good functional group tolerance, affording pharmaceutically useful 2-acyl pyridines. The electron paramagnetic resonance (EPR) studies together with control experiments showed that the singlet oxygen (1O2) and superoxide anion (O2˙?) are the reactive oxidants. The1O2generation mechanism correlated well with the photophysical properties of the substrate (Z)-triaryl-substituted alkenes, the excited state of which was proved to serve as the triplet sensitizer for the generation of1O2
Heterocyclization of enediynes promoted by sodium azide: A case of ambiguity of x-ray data and structure revision
Gulevskaya, Anna V.,Tyaglivy, Alexander S.,Pozharskii, Alexander F.,Nelina-Nemtseva, Julia I.,Steglenko, Dmitry V.
supporting information, p. 1582 - 1585 (2014/04/17)
It has been shown that contrary to the literature data the tandem cyclization of (Z)-1-aryl-3-hexen-1,5-diynes promoted by sodium azide results in the formation of the corresponding [1,2,3]triazolo[1,5-a]pyridines, not 1H-benzotriazole derivatives. Apparently, incorrect structure elucidation made by previous investigators originates from misinterpretation of X-ray data. A number of new transformations of this type as well as X-ray and NMR experiments are discussed.