Fries rearrangement takes place with esters of αβ-hexenic acid and β-isopropylacrylic acid, but no identifiable product could be isolated from the corresponding reaction with oleic acid
Fries rearrangements of 5-methyl-, 5-bromo-, and 5-chloro-2-acetoxytenzoic acids have teen effected,...
H-1, H-2, and B-11 NMR spectroscopy has been used to study the mechanism of the Fries rearrangement ...
Six esters of phenol, o-,m- and p-cresols, 1-and 2-naphthols with Cyclohexane butyric acid were pre...
Several o-hydroxy-ketones have been prepared by the Fries rearrangement of esters of αβ-nonenoic aci...
Fries rearrangement of various substituted phenolic esters of crotonic acid has been studied
The reaction temperature, nature and amount of the catalyst, nature of the solvent, and nature and s...
The Fries Reaction of some 7-acetoxy,-6-acetoxy,-7: 8-diacetoxy and 6: 7-diacetoxy coumarins has bee...
The Fries rearrangement of methyl .2 : 6-diacetoxy- as well as -dibenzoyloxy-benzoate yields methyl ...
The effet of less than a molar proportion of anhydrous aluminium chloride as a catalyst in the Fries...
The Fries rearrangement of the esters of 7-hydroxy-3-alkyl-4-methyl-6-ethylcoumarins has been studie...
The Fries rearrangement of five esters of carvacrol has been studied. the \(o\)-hydroryketones obtai...
The Fries migration has been carried out in the case of six esters of \(cyc\)lohexanepropionic acid ...
Fries isomerisation of acyl esters of o- and p-hydroxy-acetophenones to 2-hydroxy-3--acetylacetophe...
ABSTRACT- In continuation of our interest in the synthesis of biologically active, natu-ral and synt...
A study has been undertaken of the published literature on the Fries rearrangement, thermal, photo a...
Fries rearrangements of 5-methyl-, 5-bromo-, and 5-chloro-2-acetoxytenzoic acids have teen effected,...
H-1, H-2, and B-11 NMR spectroscopy has been used to study the mechanism of the Fries rearrangement ...
Six esters of phenol, o-,m- and p-cresols, 1-and 2-naphthols with Cyclohexane butyric acid were pre...
Several o-hydroxy-ketones have been prepared by the Fries rearrangement of esters of αβ-nonenoic aci...
Fries rearrangement of various substituted phenolic esters of crotonic acid has been studied
The reaction temperature, nature and amount of the catalyst, nature of the solvent, and nature and s...
The Fries Reaction of some 7-acetoxy,-6-acetoxy,-7: 8-diacetoxy and 6: 7-diacetoxy coumarins has bee...
The Fries rearrangement of methyl .2 : 6-diacetoxy- as well as -dibenzoyloxy-benzoate yields methyl ...
The effet of less than a molar proportion of anhydrous aluminium chloride as a catalyst in the Fries...
The Fries rearrangement of the esters of 7-hydroxy-3-alkyl-4-methyl-6-ethylcoumarins has been studie...
The Fries rearrangement of five esters of carvacrol has been studied. the \(o\)-hydroryketones obtai...
The Fries migration has been carried out in the case of six esters of \(cyc\)lohexanepropionic acid ...
Fries isomerisation of acyl esters of o- and p-hydroxy-acetophenones to 2-hydroxy-3--acetylacetophe...
ABSTRACT- In continuation of our interest in the synthesis of biologically active, natu-ral and synt...
A study has been undertaken of the published literature on the Fries rearrangement, thermal, photo a...
Fries rearrangements of 5-methyl-, 5-bromo-, and 5-chloro-2-acetoxytenzoic acids have teen effected,...
H-1, H-2, and B-11 NMR spectroscopy has been used to study the mechanism of the Fries rearrangement ...
Six esters of phenol, o-,m- and p-cresols, 1-and 2-naphthols with Cyclohexane butyric acid were pre...