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Buchwald-Hartwig Pd -catalyzed

The first total synthesis of (-)-fumiquinazoline A and B was accomplished by B.B. Snider and co-workers using a Buchwald-Hartwig Pd-catalyzed cyclization of an iodoindole carbamate to construct the imidazoindolone moiety. In order to set up the stereochemistry at the benzylic position of the indole fragment, the double bond was oxidized with the saccharine-derived Davis oxaziridine in the presence of methanol to give the major diastereomer in 65% yield. [Pg.131]

The Buchwald-Hartwig Pd-catalyzed aryl C—N bond formation... [Pg.21]


See other pages where Buchwald-Hartwig Pd -catalyzed is mentioned: [Pg.619]    [Pg.17]   


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