Chemistry, Ames Laboratory
Journal or Book Title
A variety of nucleophiles react efficiently with in situ generated nitroquinones. The reaction with substituted resorcinols led to the direct synthesis of the phenanthroviridinone and lagumycin skeleton via a highly regioselective Diels–Alder reaction.
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American Chemical Society
Yu, Huangchao; Fought, Ellie; Windus, Theresa L.; and Kraus, George A., "Direct Synthesis of the Phenanthroviridone Skeleton Using a Highly Regioselective Nitroquinone Diels–Alder Reaction" (2020). Chemistry Publications. 1271.