Issue 0, 1968

Structures and stereochemistry of some halogeno-derivatives of aucubin

Abstract

Halogenation of hexa-acetylaucubin in acetic acid or alcohols gives halogenoacetoxy- or halogenoalkoxy-derivatives. The differences in stereochemistry between these are explained in terms of a pathway involving conformational inversion.

Article information

Article type
Paper

J. Chem. Soc. C, 1968, 1661-1663

Structures and stereochemistry of some halogeno-derivatives of aucubin

P. W. Le Quesne, J. Chem. Soc. C, 1968, 1661 DOI: 10.1039/J39680001661

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