Macrocyclic vs. [2]catenane btp structures: influence of (aryl) substitution on the self templation of btp ligands in macrocyclic synthesis-Reference-Cited by-同舟云学术

Macrocyclic vs. [2]catenane btp structures: influence of (aryl) substitution on the self templation of btp ligands in macrocyclic synthesis

Published:2021 Issue:46 Volume:19 Page:10189-10200
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

McCarney Eoin P.¹,McCarthy William J.¹,Lovitt June I.¹²^ORCID,Gunnlaugsson Thorfinnur¹²^ORCID

Affiliation:

1. School of Chemistry and Trinity Biomedical Sciences Institute (TBSI), Trinity College Dublin, The University of Dublin, Dublin 2, Ireland

2. SFI Synthesis and Solid State Pharmaceutical Centre (SSPC), Trinity College Dublin, The University of Dublin, Dublin 2, Ireland

Abstract

The synthesis of four 2,6-bis(1,2,3-triazol-4-yl)pyridine(btp) olefin based ligands 3, 4, 11 and 12 is described and their formation of macrocyclic products using ring closing metatheses (RCM) reactions rather than mechanically interlocked molecules.

Funder

Science Foundation Ireland

Irish Research Council

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB02032C

Reference81 articles.

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5. Pillararenes, A New Class of Macrocycles for Supramolecular Chemistry

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