Tetrahedron Letters p. 381 - 384 (1994)
Update date:2022-08-30
Topics:
Georg, Gunda I.
Wu, Zhijun
(R)-(+)-1-(1-Naphthyl)ethylimines were found to be moderately better chiral templates in the Staudinger reaction in comparison to (R)-(+)-1-(phenyl)ethylimines. The best diastereoselectivities and yields were obtained with (R)-(+)-1-(1-naphthyl)ethylimine
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