In 2019.0 CHEM-EUR J published article about FRIEDEL-CRAFTS REACTIONS; PI-ACTIVATED ALCOHOLS; NUCLEOPHILIC-SUBSTITUTION; ALLYLIC ALCOHOLS; MILD; MITSUNOBU; DERIVATIVES; AMINATION; TRIFLATE; AMINES in [Estopina-Duran, Susana; Donnelly, Liam J.; Mclean, Euan B.; Hockin, Bryony M.; Slawin, Alexandra M. Z.; Taylor, James E.] Univ St Andrews, EaStCHEM, Sch Chem, St Andrews KY16 9ST, Fife, Scotland; [Taylor, James E.] Univ Bath, Dept Chem, Bath BA2 7AY, Avon, England in 2019.0, Cited 58.0. The Name is 3-Pyridinecarboxaldehyde. Through research, I have a further understanding and discovery of 500-22-1. Product Details of 500-22-1
A combination of pentafluorophenylboronic acid and oxalic acid catalyses the dehydrative substitution of benzylic alcohols with a second alcohol to form new C-O bonds. This method has been applied to the intermolecular substitution of benzylic alcohols to form symmetrical ethers, intramolecular cyclisations of diols to form aryl-substituted tetrahydrofuran and tetrahydropyran derivatives, and intermolecular crossed-etherification reactions between two different alcohols. Mechanistic control experiments have identified a potential catalytic intermediate formed between the aryl boronic acid and oxalic acid.
Product Details of 500-22-1. Bye, fridends, I hope you can learn more about C6H5NO, If you have any questions, you can browse other blog as well. See you lster.
Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem