We report a catalytic system for the challenging enantioselective addition of aryl Grignard reagents to ketones. Using a simple, one-pot procedure under mild conditions, a wide range of aromatic ketones are converted into diaryl alcohols in good yields and with good enantioselectivities.The authors acknowledge financial support from the Spanish Ministerio de Ciencia y Tecnología (MCYT) (project numbers CTQ2007-65218/BQU and CTQ2011-24151), Consolider Ingenio 2010 (grant number CSD2007-00006), and Generalitat Valenciana (G. V. PROMETEO/2009/039 and FEDER). B. M. thanks the European Commision for a Marie Curie Career Integration Grant. E. F.-M. thanks the Ministerio de Educación y Ciencia (MEC) for a FPU predoctoral fellowship (AP-2010-2926)
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
A copper(I) catalyst with a chiral ferrocenyl diphosphine ligand facilitates the additive-free 1,2-a...
Tertiary diarylmethanols are highly bioactive structural motifs. A new strategy to access chiral ter...
The enantioselective addition of Grignard reagents to ketones was promoted by a BINOL derivative bea...
© 2016 American Chemical Society.Remarkable progress in the enantioselective addition of Grignard re...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
A copper(I) catalyst with a chiral ferrocenyl diphosphine ligand facilitates the additive-free 1,2-a...
Tertiary diarylmethanols are highly bioactive structural motifs. A new strategy to access chiral ter...
The enantioselective addition of Grignard reagents to ketones was promoted by a BINOL derivative bea...
© 2016 American Chemical Society.Remarkable progress in the enantioselective addition of Grignard re...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
A copper(I) catalyst with a chiral ferrocenyl diphosphine ligand facilitates the additive-free 1,2-a...
Tertiary diarylmethanols are highly bioactive structural motifs. A new strategy to access chiral ter...