Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5271525 | Tetrahedron Letters | 2009 | 4 Pages |
A new family of achiral 3,3â²,5,5â²-tetrasubstituted-2,2â²,6,6â²-tetrahydroxy biphenyl ligand 4 was developed. The axial chirality of the ligand could be induced by the chelation of 2,2â²,6,6â²-tetrahydroxy groups with (R)-BINOL-Ti(OiPr)2 to form an axially chiral bimetallic titanium catalyst 9. Compared with (R)-BINOL-Ti(OiPr)2 catalyst, this novel catalyst 9 exhibited excellent activity and enantioselectivity for the carbonyl-ene reaction of methylstyrene and ethyl glyoxylate. 3,3â²,5,5â²-Tetrasubstituted groups showed a remarkable effect on both enantioselectivity and yield. With 9d prepared from 3,3â²,5,5â²-tetramethyl-2,2â²,6,6â²-tetrahydroxy biphenyl 4d as the catalyst, the best result, up to 97.6% ee and 99% yield, was obtained. Additionally, the bimetallic catalyst 9 also showed better catalytic capability than the corresponding monometallic catalyst.
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