Issue 0, 1971

Methyl proton resonance in nuclear magnetic resonance spectra of 2,2′- and 8,8′-dimethyl-1,1′-binaphthyls. The optical stability of (+)-2,2′-dimethyl-1,1′-binaphthyl

Abstract

(+)-2,2′-Dimethyl-1,1′-binaphthyl has resisted racemisation in solution. This contrasts with 8,8′-dimethyl-1,1′-binaphthyl which is optically labile. Methyl proton signals in the n.m.r. spectra of these compounds can be used to throw light on their conformations in the ground state.

Article information

Article type
Paper

J. Chem. Soc. B, 1971, 775-778

Methyl proton resonance in nuclear magnetic resonance spectra of 2,2′- and 8,8′-dimethyl-1,1′-binaphthyls. The optical stability of (+)-2,2′-dimethyl-1,1′-binaphthyl

W. Dixon, M. M. Harris and R. Z. Mazengo, J. Chem. Soc. B, 1971, 775 DOI: 10.1039/J29710000775

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