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Other Amino Acids as Asymmetric Organocatalysts

VINCENT COEFFARD, CHRISTINE GRECK, XAVIER MOREAU AND CHRISTINE THOMASSIGNY [Pg.297]

Institut Lavoisier de Versailles, UMR CNRS 8180, Universite de Versailles-St-Quentin-en-Yvelines, 45 Avenue des Etats-Unis, [Pg.297]

78035 Versailles cedex, France Email christine.greck uvsq.fr [Pg.297]

The aldol addition is known as one of the most important carbon-carbon bond-forming reactions, leading to a p-hydro y carbonyl structural unit which is frequently found in bioactive molecules. The seminal works in [Pg.297]

Sustainable Catalysis Without Metals or Other Endangered Elements, Part 1 [Pg.297]


See other pages where Other Amino Acids as Asymmetric Organocatalysts is mentioned: [Pg.297]    [Pg.299]    [Pg.301]    [Pg.303]    [Pg.307]   


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A asymmetric

Acidic organocatalysts

Amino acid other

Amino acids organocatalyst

Amino organocatalysts

Asymmetric organocatalysts

Organocatalysts amino acids

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