Chiral Brønsted acid catalyzed enantioselective hydrophosphonylation of imines: asymmetric synthesis of alpha-amino phosphonates.

Chiral Brønsted acid catalyzed enantioselective hydrophosphonylation of imines: asymmetric synthesis of alpha-amino phosphonates.

Organic letters (2005-06-17)

Takahiko Akiyama, Hisashi Morita, Junji Itoh, Kohei Fuchibe

ZUSAMMENFASSUNG

[reaction: see text] A cyclic phosphoric acid derivative, derived from (R)-BINOL, was used as a chiral Brønsted acid (10 mol %) in hydrophosphonylation of aldimines with diisopropyl phosphite at room temperature. Alpha-amino phosphonates were obtained with good to high enantioselectivities.

MATERIALIEN

Produktnummer

Marke

Produktbeschreibung

674605

Sigma-Aldrich

(R)-3,3′-Bis[3,5-bis(trifluormethyl)phenyl]-1,1′-binaphthyl-2,2′-diyl-Hydrogenphosphat, 95%