Tertiary diarylmethanols are highly bioactive structural motifs. A new strategy to access chiral tertiary diarylmethanols through copper-catalyzed direct alkylation of (di)(hetero)aryl ketones by using Grignard reagents was developed. The low reactivity and the similarity of the enantiotopic faces of bis-aromatic ketones were partially overcome, which resulted in moderate to good yields and enantioselectivities.</p
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...
The first catalytic enantioselective 1,2-addition of Grignard reagents to ketones is presented. This...
Tertiary diarylmethanols are highly bioactive structural motifs. A new strategy to access chiral ter...
Tertiary diarylmethanols are highly bioactive structural motifs. A new strategy to access chiral ter...
Tertiary diarylmethanols are highly bioactive structural motifs. A new strategy to access chiral ter...
The highly enantioselective addition of Grignard reagents to acylsilanes is catalyzed by copper diph...
The highly enantioselective addition of Grignard reagents to acylsilanes is catalyzed by copper diph...
The highly enantioselective addition of Grignard reagents to acylsilanes is catalyzed by copper diph...
The highly enantioselective addition of Grignard reagents to acylsilanes is catalyzed by copper diph...
Tertiary diarylmethanols are highly bioactive structural motifs. A new strategy to access chiral ter...
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...
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...
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...
The first catalytic enantioselective 1,2-addition of Grignard reagents to ketones is presented. This...
Tertiary diarylmethanols are highly bioactive structural motifs. A new strategy to access chiral ter...
Tertiary diarylmethanols are highly bioactive structural motifs. A new strategy to access chiral ter...
Tertiary diarylmethanols are highly bioactive structural motifs. A new strategy to access chiral ter...
The highly enantioselective addition of Grignard reagents to acylsilanes is catalyzed by copper diph...
The highly enantioselective addition of Grignard reagents to acylsilanes is catalyzed by copper diph...
The highly enantioselective addition of Grignard reagents to acylsilanes is catalyzed by copper diph...
The highly enantioselective addition of Grignard reagents to acylsilanes is catalyzed by copper diph...
Tertiary diarylmethanols are highly bioactive structural motifs. A new strategy to access chiral ter...
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...
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...
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...
The first catalytic enantioselective 1,2-addition of Grignard reagents to ketones is presented. This...