Literature DB >> 32201870

A highly substituted pyrazinophane generated from a quinoidal system via a cascade reaction.

Christopher L Anderson1, Jiatao Liang1, Simon J Teat2, Andrés Garzón-Ruiz3, David P Nenon4, Amparo Navarro5, Yi Liu6.   

Abstract

The generation of a highly-substituted [2.2](2,5)pyrazinophane via a cascade reaction is presented. The pyrazinophane product is formed via the dimerization of a member of the para-azaquinodimethane (p-AQM) family of conjugated quinoidal compounds-reactivity that sheds light on the nature of stability in p-AQMs. Additionally, the electronic and structural nature of this highly-strained ring system are characterized.

Entities:  

Year:  2020        PMID: 32201870     DOI: 10.1039/d0cc00916d

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


  1 in total

1.  Regiocontrolled dimerization of asymmetric diazaheptacene derivatives toward X-shaped porous semiconductors.

Authors:  Guowei Zhang; Ning Xue; Wen Gu; Xingzhou Yang; Aifeng Lv; Yonghao Zheng; Lei Zhang
Journal:  Chem Sci       Date:  2020-09-16       Impact factor: 9.825

  1 in total

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