Issue 6, 1998

Enantiopure 3-amido or 3,3′-bisamido substituted 1,1′-bi-2-naphthols by anionic Fries rearrangements

Abstract

Mono- or di-carbamates of 1,1′-bi-2-naphthol ortholithiate with Bus Li–TMEDA. The resulting anions may either be captured by MeI or allowed to undergo anionic Fries rearrangement. Thus generalised two-step routes to mono- and di-(3-alkyl) or -(3-amido) substituted 2,2′-binapthols is demonstrated.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1998, 1081-1086

Enantiopure 3-amido or 3,3′-bisamido substituted 1,1′-bi-2-naphthols by anionic Fries rearrangements

M. R. Dennis and S. Woodward, J. Chem. Soc., Perkin Trans. 1, 1998, 1081 DOI: 10.1039/A708436F

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