Regioselective SNAr reaction of the phenoxathiin-based thiacalixarene as a route to a novel macrocyclic skeleton-Reference-Cited by-同舟云学术

Regioselective SNAr reaction of the phenoxathiin-based thiacalixarene as a route to a novel macrocyclic skeleton

Published:2020 Issue:1 Volume:56 Page:78-81
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Landovský Tomáš¹²³⁴⁵,Eigner Václav⁶⁷⁴⁵^ORCID,Babor Martin⁶⁷⁴⁵^ORCID,Tichotová Markéta⁸⁷⁴⁵,Dvořáková Hana⁸⁷⁴⁵^ORCID,Lhoták Pavel¹²³⁴⁵^ORCID

Affiliation:

1. Department of Organic Chemistry

2. University of Chemistry and Technology

3. Prague (UCTP)

4. 166 28 Prague 6

5. Czech Republic

6. Department of Solid State Chemistry

7. UCTP

8. Laboratory of NMR Spectroscopy

Abstract

The formation of a novel type of macrocyclic skeleton possessing meta- and para-bridging units can be achieved by S_NAr cleavage of an easily accessible phenoxathiin-based thiacalix[4]arene.

Funder

Ministerstvo Školství, Mládeže a Tělovýchovy

Grantová Agentura České Republiky

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/C9CC08335A

Reference23 articles.

1. Recent developments of thiacalixarene based molecular motifs

2. Thiacalixarenes

3. Chemistry of Thiacalixarenes

4. Calixarenes and Beyond , ed. P. Neri , J. L. Sessler and M. X. Wang , Springer Int. Publishing , Switzerland , 2016

5. C. D. Gutsche , Calixarenes An introduction , The Royal Society of Chemistry , Thomas Graham House, Cambridge , 2nd edn, 2008

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