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

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.

Description

Only IISERM authors are available in the record.

Citation

Chemical Communications, 58(93), 12967-12970

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