Literature DB >> 20020696

Facile synthesis of 2,6-disubstituted benzobisthiazoles: functional monomers for the design of organic semiconductors.

Jared F Mike1, Jeremy J Inteman, Arkady Ellern, Malika Jeffries-EL.   

Abstract

The synthesis of several synthetically useful 2,6-disubstituted benzobisthiazoles is described. The method is based on the Lewis acid-catalyzed ring-closing reaction between substituted orthoesters and diamino benzene dithiol. The resulting benzobisthiazoles are obtained cleanly and in good yields. These materials are of interest for the development of new organic semiconductors.

Entities:  

Year:  2010        PMID: 20020696     DOI: 10.1021/jo9023864

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Structural and Spectral Analyses of 2-[(2-Benzothiazolylmethyl)thio]-benzenamine and 2-[(2-Benzothiazolylmethyl)thio]-benzenamine hydrobromide.

Authors:  Dustin W Demoin; Charles L Barnes; Timothy J Hoffman; Silvia S Jurisson
Journal:  J Chem Crystallogr       Date:  2011-02-04       Impact factor: 0.603

Review 2.  Applications of alkyl orthoesters as valuable substrates in organic transformations, focusing on reaction media.

Authors:  Zahra Khademi; Kobra Nikoofar
Journal:  RSC Adv       Date:  2020-08-17       Impact factor: 4.036

  2 in total

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