Literature DB >> 23727778

Concise synthesis of heterocycle-fused naphthoquinones by employing sonogashira coupling and tandem addition-elimination/intramolecular cyclization.

Kazunori Ueda1, Mitsuaki Yamashita, Koichi Sakaguchi, Harukuni Tokuda, Akira Iida.   

Abstract

A concise method for the synthesis of heterocycle-fused naphthoquinones such as naphtho[2,3-b]-furan-4,9-dione, 1H-benz[f]indole-4,9-dione, and naphtho[2,3-b]thiophene-4,9-dione was developed. This method employed Sonogashira coupling and tandem addition-elimination/intramolecular cyclization, and it enabled the preparation of versatile heterocycle-fused naphthoquinones from one substrate.

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Year:  2013        PMID: 23727778     DOI: 10.1248/cpb.c13-00102

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  2 in total

1.  Ultrasound assisted one-pot synthesis of benzo-fused indole-4, 9-dinones from 1,4-naphthoquinone and α-aminoacetals.

Authors:  Quang H Luu; Jorge D Guerra; Cecilio M Castañeda; Manuel A Martinez; Jong Saunders; Benjamin A Garcia; Brenda V Gonzales; Anushritha R Aidunuthula; Shizue Mito
Journal:  Tetrahedron Lett       Date:  2016-04-16       Impact factor: 2.415

2.  A new and efficient procedure for the synthesis of hexahydropyrimidine-fused 1,4-naphthoquinones.

Authors:  Marcelo Isidoro P Reis; Vinícius R Campos; Jackson A L C Resende; Fernando C Silva; Vitor F Ferreira
Journal:  Beilstein J Org Chem       Date:  2015-07-22       Impact factor: 2.883

  2 in total

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