Azobenzene-based unnatural amino acid scaffolds via a Pd(ii)-catalyzed C(sp3)–H arylation strategy?
Chemical Communications Pub Date: 2022-10-26 DOI: 10.1039/D2CC04870A
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.
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Journal Name：Chemical Communications
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CAS no.: 89640-58-4
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