Direct asymmetric aldol reactions at the less substituted carbon atom of unmodified unsymmetrical ketones are achieved in the presence of the commercially available aldolase I antibody 84G3 [Eq. (1)]. All the reactions proceeded with enantiomeric excesses greater than 94%. Both enantiomers are accessible by using either an aldol or a retro-aldol reaction
The direct asymmetric aldol reactions of equivalent molar amounts of aldehydes and ketones were carr...
In this Letter, a cysteine-derived prolinamide is described to act as a robust and effective organoc...
Recoverable BINAM-prolinamide derivatives, as well as L-proline, give results complementary to antib...
A catalytic regio- and enantioselective aldol reaction of various unsymmetrical methyl ketones with ...
High enantiomeric enrichment after 50% conversion: Racemates of aldols can be resolved by the title ...
Compounds 1-7 are the products formed by aldol condensation of p-nitrobenzaldehyde with a series of ...
The remarkable specificity of an antibody molecule has been used to accomplish highly selective func...
Aldolase antibody 38C2 catalyzes the enantioselective aldol cyclodehydration of 4-substituted-2,6-he...
Aldolase antibody 38C2-catalyzed resolutions of tertiary aldols were studied. Tertiary aldols proved...
This paper describes the substrate specificity, synthetic scope, and efficiency of aldolase catalyti...
An effective organocatalytic asymmetric aldol reaction of acetone to beta,gamma-unsaturated alpha-ke...
A diastereo- and enantioselective aldol reaction between aldehydes and a synthetically useful ketoma...
An l-pyroglutamic acid-derived bifunctional organocatalyst was designed and applied in an organocata...
Most enzymatic transformations have a synthetic counterpart. Often though, the mechanisms by which n...
Antibody catalysis has been used for the first time in a very efficient and highly enantioselective ...
The direct asymmetric aldol reactions of equivalent molar amounts of aldehydes and ketones were carr...
In this Letter, a cysteine-derived prolinamide is described to act as a robust and effective organoc...
Recoverable BINAM-prolinamide derivatives, as well as L-proline, give results complementary to antib...
A catalytic regio- and enantioselective aldol reaction of various unsymmetrical methyl ketones with ...
High enantiomeric enrichment after 50% conversion: Racemates of aldols can be resolved by the title ...
Compounds 1-7 are the products formed by aldol condensation of p-nitrobenzaldehyde with a series of ...
The remarkable specificity of an antibody molecule has been used to accomplish highly selective func...
Aldolase antibody 38C2 catalyzes the enantioselective aldol cyclodehydration of 4-substituted-2,6-he...
Aldolase antibody 38C2-catalyzed resolutions of tertiary aldols were studied. Tertiary aldols proved...
This paper describes the substrate specificity, synthetic scope, and efficiency of aldolase catalyti...
An effective organocatalytic asymmetric aldol reaction of acetone to beta,gamma-unsaturated alpha-ke...
A diastereo- and enantioselective aldol reaction between aldehydes and a synthetically useful ketoma...
An l-pyroglutamic acid-derived bifunctional organocatalyst was designed and applied in an organocata...
Most enzymatic transformations have a synthetic counterpart. Often though, the mechanisms by which n...
Antibody catalysis has been used for the first time in a very efficient and highly enantioselective ...
The direct asymmetric aldol reactions of equivalent molar amounts of aldehydes and ketones were carr...
In this Letter, a cysteine-derived prolinamide is described to act as a robust and effective organoc...
Recoverable BINAM-prolinamide derivatives, as well as L-proline, give results complementary to antib...