4.5 Article

Rh(III)-Catalyzed C-H Activation/Annulation of Aryl Hydroxamates with CF3-Containing α-Propargyl α-Amino Acid Derivatives

Journal

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2021, Issue 12, Pages 1883-1890

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.202100040

Keywords

Amino phosphonates; Catalysis; C− H activation; Fluorinated amino acids; Isoquinolones

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A series of new orthogonally protected alpha-CF3-substituted alpha-amino carboxylates and alpha-amino phosphonates decorated with pharmacophore isoquinolone core have been elaborated through the Rh(III)-catalyzed C-H activation/annulation of aryl hydroxamates with propargyl-containing alpha-amino acid derivatives and their phosphorus analogues.
A series of new orthogonally protected alpha-CF3-substituted alpha-amino carboxylates, and alpha-amino phosphonates decorated with pharmacophore isoquinolone core has been elaborated through the Rh(III)-catalyzed C-H activation/annulation of aryl hydroxamates with propargyl-containing alpha-amino acid derivatives and their phosphorus analogues.

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