Transformations of anilides of 3-aryl-2,3-epoxypropionic acids when exposed to acidic agents

Anilides of 3-aryl-2,3-epoxypropionic acids on treatment with aqueous HBr gave 3-aryl-3-bromo-2-hydroxypropionic acid anilides and (in some cases) 2-bromo-3-hydroxy regioisomers. Cyclization of these products into 3-arylquinolin-2(1 H )-ones was studied.

Saved in:
Bibliographic Details
Published in:Russian chemical bulletin Vol. 64; no. 12; pp. 2857 - 2864
Main Authors: Mamedov, V. A., Mamedova, V. L., Khikmatova, G. Z., Samigullina, A. I., Gubaidullin, A. T., Bazanova, O. B., Rizvanov, I. Kh, Sinyashin, O. G.
Format: Journal Article
Language:English
Published: New York Springer US 01-12-2015
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Anilides of 3-aryl-2,3-epoxypropionic acids on treatment with aqueous HBr gave 3-aryl-3-bromo-2-hydroxypropionic acid anilides and (in some cases) 2-bromo-3-hydroxy regioisomers. Cyclization of these products into 3-arylquinolin-2(1 H )-ones was studied.
ISSN:1066-5285
1573-9171
DOI:10.1007/s11172-015-1238-2