Issue 9, 1994

A convenient asymmetric synthesis of anti-β-amino alcohols: an X-ray crystallographic study of (4R)-2,2-dimethyl-4-[(2S)-(diphenylmethyleneamino)-(1S)-hydroxy-3-buten-1-yl]-1,3-dioxolane

Abstract

anti-β-Diphenylmethyleneamino alcohols have been produced with high relative and absolute sterocontrol in a one-pot process; subsequent deprotection gave anti-β-hydroxy amines in good yield.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 1053-1054

A convenient asymmetric synthesis of anti-β-amino alcohols: an X-ray crystallographic study of (4R)-2,2-dimethyl-4-[(2S)-(diphenylmethyleneamino)-(1S)-hydroxy-3-buten-1-yl]-1,3-dioxolane

A. G. M. Barrett, M. A. Seefeld and D. J. Williams, J. Chem. Soc., Chem. Commun., 1994, 1053 DOI: 10.1039/C39940001053

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