Direct Synthesis of the Phenanthroviridone Skeleton Using a Highly Regioselective Nitroquinone Diels-Alder Reaction.

ABSTRACT: 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.

SUBMITTER: Yu H 

PROVIDER: S-EPMC7191567 | biostudies-literature | 2020 Apr

REPOSITORIES: biostudies-literature