Synthesis of 2,3-Dioxy-1,4-anthraquinones Related to Tetracenomycins C and X
Donald W. Cameron, Peter G. Griffiths and Andrew G. Riches
Australian Journal of Chemistry
52(12) 1173 - 1177
Published: 1999
Abstract
The 2,3-dioxy-1,4-anthraquinones (6) and (7) have been synthesized from the 9,10-anthraquinone (19), through the anthrone (18). Quinones (6) and (7) respectively possess substituents appropriate for three of the four rings of tetracenomycins C (2) and X (3) but they did not show dienophilic properties towards the reactive diene (5). Interaction with the diene was complicated by transsilylation, as was also observed for the model quinone (25).https://doi.org/10.1071/CH99181
© CSIRO 1999