Articles with "michael additions" as a keyword



Enantiocomplementary Michael Additions of Acetaldehyde to Aliphatic Nitroalkenes Catalyzed by Proline‐Based Carboligases

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Published in 2022 at "Chembiochem"

DOI: 10.1002/cbic.202100644

Abstract: The blockbuster drug Pregabalin is widely prescribed for the treatment of painful diabetic neuropathy. Given the continuous epidemic growth of diabetes, the development of sustainable synthesis routes for Pregabalin and structurally related pharmaceutically active γ‐aminobutyric… read more here.

Keywords: enantiocomplementary michael; acetaldehyde aliphatic; additions acetaldehyde; michael additions ... See more keywords
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Biocatalytic Asymmetric Michael Additions of Nitromethane to α,β-Unsaturated Aldehydes via Enzyme-bound Iminium Ion Intermediates

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Published in 2019 at "ACS Catalysis"

DOI: 10.1021/acscatal.9b00780

Abstract: The enzyme 4-oxalocrotonate tautomerase (4-OT) exploits an N-terminal proline as main catalytic residue to facilitate several promiscuous C–C bond-forming reactions via enzyme-bound enamine intermediates. Here we show that the active site of this enzyme can… read more here.

Keywords: unsaturated aldehydes; enzyme bound; enzyme; asymmetric michael ... See more keywords
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Development of Chiral, Bifunctional Thiosquaramides: Enantioselective Michael Additions of Barbituric Acids to Nitroalkenes.

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Published in 2017 at "Journal of the American Chemical Society"

DOI: 10.1021/jacs.7b01115

Abstract: We report a general method for the synthesis of chiral thiosquaramides, a class of bifunctional catalysts not previously described in the literature. Thiosquaramides are found to be more acidic and significantly more soluble in nonpolar… read more here.

Keywords: thiosquaramides enantioselective; chiral bifunctional; enantioselective michael; bifunctional thiosquaramides ... See more keywords
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A thiourea-functionalized metal-organic macrocycle for the catalysis of Michael additions and prominent size-selective effect.

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Published in 2017 at "Dalton transactions"

DOI: 10.1039/c6dt04299f

Abstract: A discrete tetranuclear thiourea-based metal-organic macrocycle (MOM) with a large size was constructed by a well-designed organic ligand and nickel(ii) ions via self-assembly. Incorporating thiourea groups as hydrogen-bond donors into a metal-organic complex system leads… read more here.

Keywords: organic macrocycle; size; metal organic; michael additions ... See more keywords