A highly substituted pyrazinophane generated from a quinoidal system via a cascade reaction-Reference-Cited by-同舟云学术

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

Published:2020 Issue:32 Volume:56 Page:4472-4475
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Anderson Christopher L.¹²³⁴⁵^ORCID,Liang Jiatao¹²³⁴⁵^ORCID,Teat Simon J.⁶²³⁴^ORCID,Garzón-Ruiz Andrés⁷⁸⁹¹⁰¹¹^ORCID,Nenon David P.⁵¹²³⁴¹³^ORCID,Navarro Amparo¹⁴¹⁵¹⁶¹⁷¹⁸^ORCID,Liu Yi¹²³⁴^ORCID

Affiliation:

1. The Molecular Foundry

2. Lawrence Berkeley National Laboratory

3. Berkeley

4. USA

5. Department of Chemistry

6. Advanced Light Source

7. Department of Physical Chemistry

8. Faculty of Pharmacy

9. Universidad de Castilla-La Mancha

10. Cronista Francisco Ballesteros Gómez

11. 02071 Albacete

12. University of California

13. Materials Sciences Division

14. Department of Physical and Analytical Chemistry

15. Faculty of Experimental Sciences

16. Universidad de Jaén

17. Paraje las Lagunillas

18. Spain

Abstract

[2.2](2,5)pyrazinophanes are strained macrocycles exhibiting through-space electron density that are difficult to access synthetically. A highly-substituted member of this family is synthesized and characterized.

Funder

U.S. Department of Energy

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2020/CC/D0CC00916D

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5. Exclusive Formation of Bridge-Substituted [2.2]Paracyclophane by Topochemical Photocycloaddition Reaction of Unsymmetrical Substituted p-Quinodimethane

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