Derek H. R. Barton, PHILIP D. MAGNUS, Moshe N. Rosenfeld
Abstract
Diphenylseleninic anhydride (1) reacts with phenols under neutral conditions to give o- and p-hydroxylation, whereas with phenolate anions only o-hydroxylation is observed.
OpenAlex reports 22 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Diphenylseleninic anhydride (1) reacts with phenols under neutral conditions to give o- and p-hydroxylation, whereas with phenolate anions only o-hydroxylation is observed.
Key concepts: Hydroxylation, Phenols, Chemistry, Organic chemistry, Enzyme