Literature DB >> 29405588

Radical Alkyne peri-Annulation Reactions for the Synthesis of Functionalized Phenalenes, Benzanthrenes, and Olympicene.

Nikolay P Tsvetkov1, Edgar Gonzalez-Rodriguez1, Audrey Hughes1, Gabriel Dos Passos Gomes1, Frankie D White1, Febin Kuriakose1, Igor V Alabugin1.   

Abstract

Radical cyclization reactions at a peri position were used for the synthesis of polyaromatic compounds. Depending on the choice of reaction conditions and substrate, this flexible approach led to Bu3 Sn-substituted phenalene, benzanthrene, and olympicene derivatives. Subsequent reactions with electrophiles provided synthetic access to previously inaccessible functionalized polyaromatic compounds.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  alkyne benzannulation; cyclization; polyaromatic compounds; radical reactions; zigzag edge

Year:  2018        PMID: 29405588     DOI: 10.1002/anie.201712783

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

1.  Dehydrative π-extension to nanographenes with zig-zag edges.

Authors:  Dominik Lungerich; Olena Papaianina; Mikhail Feofanov; Jia Liu; Mirunalini Devarajulu; Sergey I Troyanov; Sabine Maier; Konstantin Amsharov
Journal:  Nat Commun       Date:  2018-11-12       Impact factor: 14.919

2.  Cascade Transformations of 1-R-Ethynyl-9,10-anthraquinones with Amidines: Expanding Access to Isoaporphinoid Alkaloids.

Authors:  Sergey Francevich Vasilevsky; Ol'ga Leonidovna Krivenko; Irina Vasilievna Sorokina; Dmitry Sergeevich Baev; Tatyana Genrikhovna Tolstikova; Igor V Alabugin
Journal:  Molecules       Date:  2021-11-15       Impact factor: 4.411

  2 in total

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