Sulfenylphosphinoferrocenes: Novel planar chiral ligands in enantioselective catalysis

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Abstract

Structurally well-defined transition-metal complexes of 1-phosphino-2-sulfenyl-ferrocene (Fesulphos ligands) act as highly efficient catalysts in a variety of mechanistically different transformations. Excellent enantioselectivities were achieved in Pd-catalyzed allylic substitutions, desymmetrization of meso-heterobicyclic alkenes by Pd-catalyzed addition of dialkylzinc reagents, Pd-catalyzed Diels-Alder reaction of cyclopentadiene with N-acryloyl oxazolidinones, and in Cu-catalyzed formal aza-Diels-Alder reaction of Danishefsky diene to N-sulfonyl aldimines. © 2006 IUPAC.

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Cabrera, S., García Mancheño, O., Gómez Arrayás, R., Alonso, I., Mauleón, P., & Carretero, J. C. (2006). Sulfenylphosphinoferrocenes: Novel planar chiral ligands in enantioselective catalysis. In Pure and Applied Chemistry (Vol. 78, pp. 257–265). https://doi.org/10.1351/pac200678020257

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