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Oxypalladation-reductive elimination domino

Full details for the synthesis of 2,3,5-trisubstituted furans via an oxypalladation-reductive elimination domino reaction were given <03T4661>. Under an atmosphere of CO, the reaction afforded furan derivatives widi incorporation of a carbonyl group. [Pg.171]

V.3.2.2 Oxypalladation-Reductive Elimination Domino Reactions with Organopalladium and Hydridopalladium Derivatives... [Pg.550]

The oxypalladation—reductive elimination domino reaction with organopalladium and hy-dridopaUadium derivatives provides a powerful and flexible tool for the construction of oxygen-containing rings. [Pg.566]

Arcadi,A., Cacchi, S Fabrizi, G., Marinelli, F. and Parisi, L,M. (2003) Flighty substituted flirans from 2-propynyl-l,3-dicarbonyls and organic halides or triflates via oxypalladation-reductive elimination domino reaction. Tetrahedron, 59, 4661-4671. [Pg.250]

See other pages where Oxypalladation-reductive elimination domino is mentioned: [Pg.550]    [Pg.552]    [Pg.554]    [Pg.556]    [Pg.558]    [Pg.560]    [Pg.562]    [Pg.564]    [Pg.566]    [Pg.586]    [Pg.588]   


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Oxypalladation-reductive elimination domino reactions

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