Literature DB >> 28702515

Chemoselective Ullmann coupling at room temperature: a facile access to 2-aminobenzo[b]thiophenes.

Manojkumar Janni1, Annaram Thirupathi1, Sahil Arora1, S Peruncheralathan1.   

Abstract

Various functionalized 2-aminobenzo[b]thiophenes have been synthesized at room temperature by the Ullmann coupling reaction for the first time. The enantiospecific coupling reaction has been further demonstrated without loss of optical purity. The newly synthesized 2-anilino-3-cyano-benzo[b]thiophenes are transformed into 11-amino-benzothieno[2,3-b]quinolines in the presence of triflic acid.

Entities:  

Year:  2017        PMID: 28702515     DOI: 10.1039/c7cc03273k

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Indium-Catalyzed Annulation of o-Acylanilines with Alkoxyheteroarenes: Synthesis of Heteroaryl[b]quinolines and Subsequent Transformation to Cryptolepine Derivatives.

Authors:  Kyohei Yonekura; Mika Shinoda; Yuko Yonekura; Teruhisa Tsuchimoto
Journal:  Molecules       Date:  2018-04-05       Impact factor: 4.411

2.  Synthesis and characterization of highly efficient and recoverable Cu@MCM-41-(2-hydroxy-3-propoxypropyl) metformin mesoporous catalyst and its uses in Ullmann type reactions.

Authors:  Zahra S Robatjazi; M Reza Naimi-Jamal; Mahdieh Tajbakhsh
Journal:  Sci Rep       Date:  2022-03-23       Impact factor: 4.379

  2 in total

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