A Noncoordinating Acid–Base Catalyst for the Mild and Nonreversible tert-Butylation of Alcohols and Phenols

Base (topology)
DOI: 10.1021/acs.joc.1c00193 Publication Date: 2021-03-09T13:25:02Z
ABSTRACT
A mild and nonreversible tert-butylation of alcohols phenols can be achieved in high yields using the noncoordinating acid–base catalyst [bis(trifluoromethane)sulfonimide 2,6-lutidine] with a reagent, tert-butyl 2,2,2-trichloroacetimidate. This method allows use substrates containing acid sensitive groups such as ketal, Boc, boronate esters.
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