Total reactivity of pyridine and quinoline via the reactions of arylbenzoates with hydroxide ion. Apparent substituent constants for some N-heteroaromatic groups-Reference-Cited by-同舟云学术

Total reactivity of pyridine and quinoline via the reactions of arylbenzoates with hydroxide ion. Apparent substituent constants for some N-heteroaromatic groups

Published:1981-01 Issue:47 Volume:22 Page:4733-4736
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Sawada Masami,Ichihara Masaharu,Ando Takashi,Yukawa Yasuhide,Tsuno Yuho

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference15 articles.

1. Electronic nature of the aza substituent of pyridyl and quinolyl groups for reactivities in an insulated system

2. Rate correlations involving the linear combination of substituent parameters. Part II. Hydrolysis of aryl benzoates

3. Multiple structure reactivity correlations. Alkaline hydrolyses of acyl and aryl-substituted phenyl benzoates

4. Determining second order rate constants

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