680997-63-1Relevant academic research and scientific papers
Diastereoselective dearomatization of resorcinols directed by a lactic acid tether: Unprecedented enantioselective access to p-quinols
Mejorado, Lupe H.,Hoarau, Christophe,Pettus, Thomas R. R.
, p. 1535 - 1538 (2004)
An operationally simple oxidative dearomatization of resorcinol derivatives is reported that employs an inexpensive chiral directing group. The method provides access to a variety of p-quinol derivatives in good yield and diastereoselectivity. A short red
