Literature DB >> 21963641

One-pot synthesis of benzo[f]indole-4,9-diones from 1,4-naphthoquinones and terminal acetylenes.

Mitsuaki Yamashita1, Kazunori Ueda, Koichi Sakaguchi, Harukuni Tokuda, Akira Iida.   

Abstract

In this paper, a concise one-pot method for the construction of benzo[f]indole-4,9-dione motifs is described. These transformations proceed via a sequential palladium- and copper-catalyzed coupling reaction of 1,4-naphthoquinones with terminal acetylenes, followed by a copper-catalyzed intramolecular cyclization reaction of the resulting coupling product.

Entities:  

Mesh：

Substances：

Year:  2011        PMID： 21963641     DOI： 10.1248/cpb.59.1289

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.  Naphthoquinone as a New Chemical Scaffold for Leishmanicidal Inhibitors of Leishmania GSK-3.

Authors:  Victor Sebastián-Pérez; Paula Martínez de Iturrate; Montserrat Nácher-Vázquez; Luis Nóvoa; Concepción Pérez; Nuria E Campillo; Carmen Gil; Luis Rivas
Journal:  Biomedicines       Date:  2022-05-14
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.