A zinc-/quinine-mediated enantioselective Aldol-type reaction of trifluorodiazoethane (CF3CHN2) with various aldehydes is described. This study demonstrated the feasibility of utilizing CF3CHN2 as an effective hard nucleophile in catalytic asymmetric transformations. Furthermore, the synthetic utility of this protocol is exemplified by the construction of a diverse set of chiral β-trifluoromethylated alcohols, including a valuable HDAC inhibitor precursor
A highly enantioselective Friedel–Crafts alkylation reaction of indoles with β-CF<sub>3</sub>-β-disu...
The aldol reaction is one of the most important carbon–carbon bond formations in synthetic organic c...
The enantioselective cross-aldol reaction between <i>o</i>-hydroxyacetophenones and trifluoromethyl ...
In this work, we thoroughly investigated the effect of structural differentiation of a series of N,N...
International audienceThe enantioselective construction of fluorohydrins featuring a tetrasubstitute...
International audienceThe catalytic asymmetric synthesis of α,α-difluoromethylated tertiary alcohols...
A highly enantioselective aza-Friedel–Crafts (aza-F-C) reaction of cyclic trifluoromethyl ketimines ...
The organolithium species addition to 2-hydroxymethyl fluorinated oxazolidines (Fox) provides a high...
A highly enantioselective and regioselective chiral Lewis acid catalyzed tandem Friedel–Crafts/lacto...
Aldol reactions with trifluoroacetophenones as acceptors yield chiral α-aryl, α-trifluoromethyl tert...
Fluorine is the most electronegative element in the periodic table, and the introduction of one or m...
The first direct asymmetric synthetic preparation of trifluoro-1-(indol-3-yl)ethanols (TFIEs) is des...
Biologically relevant chiral 3,3-disubstituted oxindole products containing a β-fluoroamine unit are...
The first example of a highly enantioselective vinylogous Michael-type reaction of β,β-disubstituted...
Duangdee N, Harnying W, Rulli G, Neudoerfl J-M, Gröger H, Berkessel A. Highly Enantioselective Organ...
A highly enantioselective Friedel–Crafts alkylation reaction of indoles with β-CF<sub>3</sub>-β-disu...
The aldol reaction is one of the most important carbon–carbon bond formations in synthetic organic c...
The enantioselective cross-aldol reaction between <i>o</i>-hydroxyacetophenones and trifluoromethyl ...
In this work, we thoroughly investigated the effect of structural differentiation of a series of N,N...
International audienceThe enantioselective construction of fluorohydrins featuring a tetrasubstitute...
International audienceThe catalytic asymmetric synthesis of α,α-difluoromethylated tertiary alcohols...
A highly enantioselective aza-Friedel–Crafts (aza-F-C) reaction of cyclic trifluoromethyl ketimines ...
The organolithium species addition to 2-hydroxymethyl fluorinated oxazolidines (Fox) provides a high...
A highly enantioselective and regioselective chiral Lewis acid catalyzed tandem Friedel–Crafts/lacto...
Aldol reactions with trifluoroacetophenones as acceptors yield chiral α-aryl, α-trifluoromethyl tert...
Fluorine is the most electronegative element in the periodic table, and the introduction of one or m...
The first direct asymmetric synthetic preparation of trifluoro-1-(indol-3-yl)ethanols (TFIEs) is des...
Biologically relevant chiral 3,3-disubstituted oxindole products containing a β-fluoroamine unit are...
The first example of a highly enantioselective vinylogous Michael-type reaction of β,β-disubstituted...
Duangdee N, Harnying W, Rulli G, Neudoerfl J-M, Gröger H, Berkessel A. Highly Enantioselective Organ...
A highly enantioselective Friedel–Crafts alkylation reaction of indoles with β-CF<sub>3</sub>-β-disu...
The aldol reaction is one of the most important carbon–carbon bond formations in synthetic organic c...
The enantioselective cross-aldol reaction between <i>o</i>-hydroxyacetophenones and trifluoromethyl ...