New explortion of 1,3-Dimethoxybenzene

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An article Direct Synthesis of the Phenanthroviridone Skeleton Using a Highly Regioselective Nitroquinone Diels-Alder Reaction WOS:000529926400026 published article about QUINONES in [Yu, Huangchao; Fought, Ellie L.; Windus, Theresa L.; Kraus, George A.] Iowa State Univ, Dept Chem, Ames, IA 50011 USA in 2020, Cited 15. Recommanded Product: 151-10-0. The Name is 1,3-Dimethoxybenzene. Through research, I have a further understanding and discovery of 151-10-0

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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Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com