Cyclization of 2,4‐dinitronaphth‐1‐yl amino acids and their analogues to naphthimindazol‐N‐oxides: Kinetics and mechanism

A variety of novel naphthimindazol‐N‐oxides and naphththiazol‐N‐oxide have been prepared in a simple two‐step process. The first step involves the reaction of 1‐chloro‐2,4‐dinitronaphthalene with glycine, alanine, glycolic acid, thioglycolic acid, and their methyl esters affording substitution produ...

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Veröffentlicht in:	Journal of physical organic chemistry 2024-01, Vol.37 (1), p.n/a
Hauptverfasser:	Omar, Alaa Z., Khattab, Sherine N., Ibrahim, Mahmoud F., El‐Sadany, Samir K., Hamed, Ezzat A.
Format:	Artikel
Sprache:	eng
Schlagworte:	Alanine Amino acids Esters Glycine Glycolic acid imidazol‐N‐oxide Kinetics Meisenheimer Nitrogen Reaction mechanisms second order Substitution reactions UV spectra
Online-Zugang:	Volltext
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