Extended knowledge of (R)-4-Hydroxydinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepine 4-oxide

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A highly diastereo- and enantioselective four-component reaction of a diazo ketone with two molecules of anilines and ethyl glyoxylate was achieved under Rh2(OAc)4 and chiral phosphoric acid cocatalyzed conditions. This transformation proceeds through a Mannich-type trapping of the ammonium ylide generated from metal carbene and one molecule of aniline with iminoester derived from another molecule of aniline and ethyl glyoxylate. With this method, a series of chiral alpha,beta-diamino acid derivatives were efficiently constructed in good yields and with good to excellent diastereo- and enantioselectivities. Georg Thieme Verlag Stuttgart New York.

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Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare