“…Further, 4-amino-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carbaldehyde was formed by demethylation. Ring-opening reactions lead to the formation of CO 2 , NH 3 , and other simple products, thereafter [ 52 ]. In the second route dihydroxylation leads to the formation of 3,10,12,12a-tetrahydroxy-6-methyl-3,4,4a,5a,6,12a-hexahydrotetracene-1,11(2H,5H)-dione followed by the abstraction of NCH 3 group from 4-(dimethylamino)-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamide.…”