The Effect of Geminal Substitution Ring Size and Rotamer Distribution on the Intramolecular Nucleophilic Catalysis of the Hydrolysis of Monophenyl Esters of Dibasic Acids and the Solvolysis of the Intermediate Anhydrides
The Effect of Geminal Substitution Ring Size and Rotamer Distribution on the Intramolecular Nucleophilic Catalysis of the Hydrolysis of Monophenyl Esters of Dibasic Acids and the Solvolysis of the Intermediate Anhydrides
Indirect hydroquinone succinoylation via a photo-fries rearrangement. Application to the synthesis of enol lactones.
作者:Roberto Martínez-Utrilla、Miguel Angel Miranda
DOI:10.1016/0040-4039(80)80024-4
日期:1980.1
A photo-Fries rearrangement of hydroquinone succinates is the key step that allows the preparation of some γ-aryl enol lactones by dehydration of the corresponding aroyl propionic acids.