Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has been made over the past decade. This enantioselective transformation now allows the use of these challenging reactive nucleophiles for the formation of chiral alcohols using catalytic amounts of chiral ligands. This review summarizes the developments in this area
The catalytic asymmetric synthesis of tertiary alcohols by the addition of organometallic reagents t...
The catalytic asymmetric synthesis of tertiary alcohols by the addition of organometallic reagents t...
General methods to prepare chiral N‐heterocyclic molecular scaffolds are greatly sought after becaus...
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 ...
© 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 ...
We report a catalytic system for the challenging enantioselective addition of aryl Grignard reagents...
The catalytic asymmetric synthesis of tertiary alcohols by the addition of organometallic reagents t...
The catalytic asymmetric synthesis of tertiary alcohols by the addition of organometallic reagents t...
General methods to prepare chiral N‐heterocyclic molecular scaffolds are greatly sought after becaus...
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 ...
© 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 ...
We report a catalytic system for the challenging enantioselective addition of aryl Grignard reagents...
The catalytic asymmetric synthesis of tertiary alcohols by the addition of organometallic reagents t...
The catalytic asymmetric synthesis of tertiary alcohols by the addition of organometallic reagents t...
General methods to prepare chiral N‐heterocyclic molecular scaffolds are greatly sought after becaus...