The transposing of isomer yields in the methanolyses of N-substituted quinolinimides by triethylamine

Theodorus Van Es, Benjamin Staskun, Peter Karuso

Research output: Contribution to journalArticleResearchpeer-review

Abstract

The effect of triethylamine in transposing the respective yields of the two isomeric esters ensuing from the methanolysis of N-substituted quinolinimides is described and is rationalized with a mechanism.

LanguageEnglish
Pages53-61
Number of pages9
JournalSouth African Journal of Chemistry
Volume65
Publication statusPublished - 2012

Fingerprint

Isomers
Esters
triethylamine

Cite this

@article{9ca5a79aedc14a028450fe766003602a,
title = "The transposing of isomer yields in the methanolyses of N-substituted quinolinimides by triethylamine",
abstract = "The effect of triethylamine in transposing the respective yields of the two isomeric esters ensuing from the methanolysis of N-substituted quinolinimides is described and is rationalized with a mechanism.",
author = "{Van Es}, Theodorus and Benjamin Staskun and Peter Karuso",
year = "2012",
language = "English",
volume = "65",
pages = "53--61",
journal = "South African Journal of Chemistry",
issn = "0379-4350",
publisher = "Bureau for Scientific Publications",

}

The transposing of isomer yields in the methanolyses of N-substituted quinolinimides by triethylamine. / Van Es, Theodorus; Staskun, Benjamin; Karuso, Peter.

In: South African Journal of Chemistry, Vol. 65, 2012, p. 53-61.

Research output: Contribution to journalArticleResearchpeer-review

TY - JOUR

T1 - The transposing of isomer yields in the methanolyses of N-substituted quinolinimides by triethylamine

AU - Van Es, Theodorus

AU - Staskun, Benjamin

AU - Karuso, Peter

PY - 2012

Y1 - 2012

N2 - The effect of triethylamine in transposing the respective yields of the two isomeric esters ensuing from the methanolysis of N-substituted quinolinimides is described and is rationalized with a mechanism.

AB - The effect of triethylamine in transposing the respective yields of the two isomeric esters ensuing from the methanolysis of N-substituted quinolinimides is described and is rationalized with a mechanism.

UR - http://www.scopus.com/inward/record.url?scp=84859081897&partnerID=8YFLogxK

M3 - Article

VL - 65

SP - 53

EP - 61

JO - South African Journal of Chemistry

T2 - South African Journal of Chemistry

JF - South African Journal of Chemistry

SN - 0379-4350

ER -