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Catalytic enantioselective hetero-Diels-Alder reactions of an azo compound.

Journal of the American Chemical Society (2006-12-21)
Masanori Kawasaki, Hisashi Yamamoto
ZUSAMMENFASSUNG

This communication describes studies in which an azo hetero-Diels-Alder adduct was furnished in high regio- and enantioselectivity using azopyridine as a reagent and silver as a catalyst. The obtained hetero-Diels-Alder adduct was easily converted to the corresponding chiral 1,4-diamino alcohol.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
(R)-(+)-2,2′-Bis(diphenylphosphin)-1,1′-binaphthalin, 97%