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Azobenzene-based unnatural amino acid scaffolds via a Pd(II)-catalyzed C(sp3)-H arylation strategy.

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Azobenzene-based unnatural amino acid motifs were synthesized via Pd(II)-catalyzed diastereoselective C(sp3)-H arylation of amino acid carboxamides with iodoacetanilides and Mills azo coupling. Click to show full abstract

Azobenzene-based unnatural amino acid motifs were synthesized via Pd(II)-catalyzed diastereoselective C(sp3)-H arylation of amino acid carboxamides with iodoacetanilides and Mills azo coupling.

Keywords: based unnatural; azobenzene based; amino acid; unnatural amino; amino

Journal Title: Chemical communications
Year Published: 2022

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