Synthesis of the kappa-agonist CJ-15,161 via a palladium-catalyzed cross-coupling reaction
Chemical Communications2002Iss. 15, pp. 1644–1645
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Abstract
Syntheses of CJ-15,161 (1) involving intermolecular N-arylation of an appropriately functionalized diamine, obtained from the precursor alpha-amino acids or, more conveniently, from the corresponding 1,2-amino alcohols via 1,2,3-oxathiazolidine-2,2-dioxide 22, are reported.
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