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

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      ACS Omega
      American Chemical Society

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          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.

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          Macmolplt: a graphical user interface for GAMESS

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            Total Synthesis of Phomazarin

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              Alkaloids fromPorcelia macrocarpa1

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                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                17 April 2020
                28 April 2020
                : 5
                : 16
                : 9311-9315
                Affiliations
                Department of Chemistry, Iowa State University , Ames, Iowa 50011, United States
                Author notes
                Article
                10.1021/acsomega.0c00201
                7191567
                540c10b6-bce9-49e2-9c0f-647fa6389a4b
                Copyright © 2020 American Chemical Society

                This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.

                History
                : 15 January 2020
                : 02 April 2020
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                Custom metadata
                ao0c00201
                ao0c00201

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