Regioselective Synthesis of O -Methyl Derivatives of the Trihydroxy Anthraquinones Morindone and Nataloe-Emodin
Donald W. Cameron and D. Ross Coller
Australian Journal of Chemistry
52(10) 941 - 948
Published: 1999
Abstract
Cycloaddition chemistry of dichloronaphthoquinones has led to regioselective syntheses of all regioisomeric α-O- methyl derivatives of morindone (2) and nataloe-emodin (4), including the natural anthraquinone ethers (1) and (3).https://doi.org/10.1071/CH99106
© CSIRO 1999