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(-)-(1S,2S)-(N,O-Dimethylephedrine)tricarbonyl chromium(0) (6) and (-)-(1S,2R)-(N,O-dimethylpseudoephedrine)tricarbonylchiromium(0) (22) undergo completely stereoselective ortho deprotonation upon treatment with alkyllithium base, followed by addition of an electrophile. In both cases, exclusive removal of the pro-(R)-ortho proton was confirmed by single crystal X-ray structure analyses of the methylated products. Addition of methyllithium onto the ortho-formylated derivative of complex (6) occurs stereoselectively, the stereochemistry of the major product being confirmed by a single crystal X-ray structure determination. The results presented demonstrate an efficient transfer of chirality from a side chain onto the (arene)tricarbonylchromium(0) complex and back to a different side chain. © 1990.

Original publication

DOI

10.1016/S0957-4166(00)80447-4

Type

Journal article

Journal

Tetrahedron: Asymmetry

Publication Date

01/01/1990

Volume

1

Pages

817 - 842