Hydrogen bonding and alcohol effects in asymmetric hypervalent iodine catalysis: Enantioselective oxidative dearomatization of phenols
Iodine chooses: A conformationally flexible C2-symmetric organoiodine(III) catalyst for the highly enantioselective catalytic oxidative dearomatization of phenols has been developed. Catalysis is controlled by intramolecular hydrogen-bonding interactions and additional achiral alcohols. Copyright
Uyanik, Muhammet,Yasui, Takeshi,Ishihara, Kazuaki
supporting information
p. 9215 - 9218
(2013/09/12)
More Articles about upstream products of 1452925-77-7