Issue 12, 1997

New chiral ammonium salt hosts derived from amino acids: very efficient optical resolution of 2,2′-dihydroxy-1,1′-binaphthyl by complexation with these host compounds

Abstract

Chiral ammonium salt hosts are prepared from amino acids by transformation of their NH 2 and CO 2 H groups into Me 3 N + Br - and CH 2 OH groups, respectively, via three simple reaction steps; by complexation with these hosts, 2,2′-dihydroxy-1,1′-binaphthyl is resolved very efficiently.

Article information

Article type
Paper

Chem. Commun., 1997, 1087-1088

New chiral ammonium salt hosts derived from amino acids: very efficient optical resolution of 2,2′-dihydroxy-1,1′-binaphthyl by complexation with these host compounds

F. Toda and K. Tanaka, Chem. Commun., 1997, 1087 DOI: 10.1039/A701682D

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