Product Details of 123-11-5. Authors Elinson, MN; Ryzhkova, YE; Vereshchagin, AN; Ryzhkov, FV; Egorov, MP in WILEY published article about in [Elinson, Michail N.; Ryzhkova, Yuliya E.; Vereshchagin, Anatoly N.; Ryzhkov, Fedor V.; Egorov, Mikhail P.] ND Zelinskii Inst Organ Chem, Dept Organ Chem, Leninsky Prospect 47, Moscow 119991, Russia in 2021.0, Cited 48.0. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5
The new electrocatalytic multicomponent transformation has been found: the electrolysis of arylaldehydes, N,N ‘-dimethylbarbiturate, and cycloxehane-1,3-diones in alcohols in the presence of sodium bromide as a mediator in an undivided cell results in the formation of substituted unsymmetric spirobarbituric dihydrofurans in 62%-76% yields. The optimized reaction conditions and a mechanistic rationale for this electrocatalytic multicomponent transformation are presented. This new electrocatalytic process is a facile and efficient way to produce substituted unsymmetric spirobarbituric dihydrofurans containing both barbituric and 3,5,6,7-tetrahydro-1-benzofuran-4(2H)-one fragments, which are promising compounds for different biomedical applications, among them are anticonvulsants, anti-AIDS agents, and antiinflammatory remedies. The scaffold approach was employed to find a protein, which may be influenced by the synthesized compounds-human aldose reductase was proposed. It was shown by molecular docking studies that such a scaffold search is beneficial and tetrahydro-2 ‘ H,4H-spiro[benzofuran-2,5 ‘-pyrimidines] used in this approach are promising for the development of novel aldose reductase inhibitors.
Product Details of 123-11-5. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Elinson, MN; Ryzhkova, YE; Vereshchagin, AN; Ryzhkov, FV; Egorov, MP or concate me.
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles