Literature DB >> 26705096

An Aza-Diels-Alder Approach to Crowded Benzoquinolines.

Amir Mazaheripour1, David J Dibble1, Mehran J Umerani1, Young S Park1, Robert Lopez2, Dylan Laidlaw2, Eriberto Vargas1, Joseph W Ziller2, Alon A Gorodetsky1,2.   

Abstract

Graphene nanoribbons (GNRs) are promising candidate materials for the next generation of nanoscale electronics. Described herein is the synthesis of 2,4,6-substituted benzoquinolines, which constitute building blocks for nitrogen-doped GNRs. The presented facile and modular aza-Diels-Alder chemistry accommodates the installation of diverse functionalities at the crowded benzoquinolines' 2 positions. Given the general utility of the benzoquinoline motif, these findings hold relevance not only for carbon-based electronics but also for a range of chemical disciplines.

Entities:  

Year:  2015        PMID: 26705096     DOI: 10.1021/acs.orglett.5b02939

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  1 in total

1.  An aza-Diels-Alder approach to chlorinated quinolines, benzoquinolines, and polybenzoquinolines.

Authors:  Juhwan Kim; Mehran J Umerani; Reina Kurakake; Huiting Qin; Joseph W Ziller; Alon A Gorodetsky; Young S Park
Journal:  RSC Adv       Date:  2021-04-14       Impact factor: 3.361

  1 in total

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