Additive effect of substituents and heterocyclic nitrogen on the alkaline hydrolysis rate of methyl esters of the substituted pyridinecarboxylic acids

Additive effect of substituents and heterocyclic nitrogen on the alkaline hydrolysis rate of methyl esters of the substituted pyridinecarboxylic acids Full article

Journal

Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393

Output data

Year: 1998, Volume: 34, Number: 11, Pages: 1685-1689 Pages count : 5

Authors

Sedova V.F. ¹ , Skurko O.P. ¹

Affiliations

1	(Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Division, Russian Academy of Sciences, Novosibirsk, Russian Federation

Rate constants of alkaline hydrolysis of methyl esters in six series of substituted pyridinecarboxylates additively correlate with σ-constants of the nitrogen atom in the pyridine ring and of substituents taking into account the transmission factors of their inductive and resonance effects. © 1998 MAHK "Hayka/Interperiodica".

Sedova V.F. , Skurko O.P.
Additive effect of substituents and heterocyclic nitrogen on the alkaline hydrolysis rate of methyl esters of the substituted pyridinecarboxylic acids
Russian Journal of Organic Chemistry. 1998. V.34. N11. P.1685-1689. Scopus РИНЦ

Scopus	2-s2.0-27844499398
Elibrary	13287201