Published September 1987 | Version v1
Journal article

Alkaline hydrolysis of averufin: production of 1,3,6,8-tetrahydroxyanthroquinone, and further investigations of averufin biosynthesis

  • 1. Council for Scientific and Industrial Research, Pretoria (South Africa). National Chemical Research Lab.
  • 2. National Food Research Institute, CSIR, Pretoria, South Africa

Description

The formation of 1,3,6,8-tetrahydroxyanthraquinone from alkaline hydrolysis of averufin is described. The utility of this reaction in a further investigation of averufin biosynthesis is explored. The structure of 1,3,6,8-tetrahydroxyantraquinone was based on a comparison of its physical properties and on an examination of its 1H and 13C n.m.r. chemical shifts

Additional details

Publishing Information

Journal Title
S. Afr. J. Chem.
Journal Volume
40
Journal Issue
3
Series
S. Afr. J. Chem.
Journal Page Range
204-206
ISSN
0379-4350
CODEN
SAJCD