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© 1995 Georg Thieme Verlag, Rudigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. Homochiral (1'R)-(+)-(ortho-methoxystyrene) chromium tricarbonyl undergoes a completely α-stereoselective tandem β-nucleophilic, α-electrophilic addition sequence with t-butyl lithium and methyl iodide to generate, after decomplexation, homochiral (2R)-(+)-2-(ortho-anisyl)-4,4-dimethylpentane.

Original publication

DOI

10.1055/s-1995-4865

Type

Journal article

Journal

Synlett

Publication Date

01/01/1995

Volume

1995

Pages

69 - 70