The desymmetrization of prochiral diesters with a chiral phosphoric acid catalyst to produce highly enantioenriched lactones in excellent yield is reported. The process is easily scaled and accommodates a variety of substitution patterns, many of which result in the generation of an enantioenriched all-carbon quaternary center. Manipulation of lactone product to useful small building blocks is also described
In the enzymatic asymmetric synthesis, the enzyme allows the desymmetrization of achiral compounds r...
The enantioselective reduction of prochiral 4,4-disubstituted 2,5-cyclohexadienones to chiral 2-cyc...
A polystyrene-supported BINOL-derived chiral phosphoric acid has been applied to the desymmetrisatio...
International audienceMeso compounds represent a particular family of achiral molecules bearing elem...
A novel method to desymmetrize <i>meso</i>-anhydrides into lactones via asymmetric hydrogenation cat...
Wring it out: The title reaction proceeds in the presence of chiral Brønsted acid catalysts. This ef...
Asymmetric bromolactonizations of alkynes are possible using a desymmetrization approach. The commer...
Catalytic asymmetric desymmetrization represents an excellent strategy for accessing highly function...
International audienceThe symmetry breaking of meso primary diols bearing a tetrahydropyran ring was...
The enantioselective desymmetrization is regarded as an effective strategy for producing chiral comp...
The asymmetric total synthesis of (−)-leuconoxine has been achieved. The desymmetrization of a proch...
Catalytic enantioselective strategies have become synthetically useful to access P-stereogenic phosp...
This review covers the recent developments (since 2015) of enantioselective desymmetrization reactio...
The gold(I)-catalyzed enantioselective hydroetherification of alkynes was achieved via desymmetriza...
International audienceThe enantioselective enzymatic desymmetrization of several highly substituted ...
In the enzymatic asymmetric synthesis, the enzyme allows the desymmetrization of achiral compounds r...
The enantioselective reduction of prochiral 4,4-disubstituted 2,5-cyclohexadienones to chiral 2-cyc...
A polystyrene-supported BINOL-derived chiral phosphoric acid has been applied to the desymmetrisatio...
International audienceMeso compounds represent a particular family of achiral molecules bearing elem...
A novel method to desymmetrize <i>meso</i>-anhydrides into lactones via asymmetric hydrogenation cat...
Wring it out: The title reaction proceeds in the presence of chiral Brønsted acid catalysts. This ef...
Asymmetric bromolactonizations of alkynes are possible using a desymmetrization approach. The commer...
Catalytic asymmetric desymmetrization represents an excellent strategy for accessing highly function...
International audienceThe symmetry breaking of meso primary diols bearing a tetrahydropyran ring was...
The enantioselective desymmetrization is regarded as an effective strategy for producing chiral comp...
The asymmetric total synthesis of (−)-leuconoxine has been achieved. The desymmetrization of a proch...
Catalytic enantioselective strategies have become synthetically useful to access P-stereogenic phosp...
This review covers the recent developments (since 2015) of enantioselective desymmetrization reactio...
The gold(I)-catalyzed enantioselective hydroetherification of alkynes was achieved via desymmetriza...
International audienceThe enantioselective enzymatic desymmetrization of several highly substituted ...
In the enzymatic asymmetric synthesis, the enzyme allows the desymmetrization of achiral compounds r...
The enantioselective reduction of prochiral 4,4-disubstituted 2,5-cyclohexadienones to chiral 2-cyc...
A polystyrene-supported BINOL-derived chiral phosphoric acid has been applied to the desymmetrisatio...