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Efficient synthesis of functionalized α-aryl α-aminoesters via reaction of polyfunctional diarylzincs with a glycine cation equivalent
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Efficient synthesis of functionalized α-aryl α-aminoesters via reaction of polyfunctional diarylzincs with a glycine cation equivalent

Frédéric Lamaty, René Lazaro et Jean Martinez
Tetrahedron letters, Vol.38(19), pp.3385-3386
12/05/1997

Résumé

Functionalized diarylzinc reagents, easily available from the corresponding aryl halides by a halogen-lithium exchange followed by transmetalation with ZnCl 2 react with a glycine cation equivalent to afford substituted α-aryl α-amino esters in good yields. Functionalized diarylzinc reagents react with a glycine cation equivalent to afford substituted α-aryl α-aminoesters in good yields.

Indicateurs

1 Consultations de la notice

Détails

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