Two-step synthesis of ferrocenyl esters of vanillic acid

Autor:	M. S. Denisov, Vladimir A. Glushkov, L. V. Pavlogradskaya, V. O. Nebogatikov, A. A. Gorbunov
Rok vydání:	2017
Předmět:	010405 organic chemistry Vanillin chemistry.chemical_element General Chemistry 010402 general chemistry 01 natural sciences Oxygen Copper 0104 chemical sciences Catalysis chemistry.chemical_compound chemistry Vanillic acid Phenol Organic chemistry Sulfate Cytotoxicity
Zdroj:	Russian Journal of General Chemistry. 87:463-469
ISSN:	1608-3350 1070-3632
DOI:	10.1134/s107036321703015x
Popis:	Successive reactions of vanillin with aromatic aldehydes at the phenol group and ferroceneboronic acid at the carbonyl group catalyzed with various N-heterocyclic carbenes afforded the corresponding ferrocenyl esters. In these reactions copper(II) sulfate, cinnamic aldehyde, and air oxygen act as oxidants. The resulting ferrocenyl esters of vanillic acid were tested for cytotoxicity.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::1c88ed536671d1a8360f2e3698b341d9 https://doi.org/10.1134/s107036321703015x Zobrazit plný text záznamu Plný text ve formátu PDF