Cargando…

Competitive formation of homocircuit [3]rotaxanes in synthetically useful yields in the bipyridine-mediated active template CuAAC reaction

We recently identified competitive formation of doubly interlocked [3]rotaxanes as the origin of the non-linear variation in yield of [2]rotaxane with macrocycle size in the bipyridine-mediated AT-CuAAC reaction. Selection of reaction conditions gave [2]rotaxanes in essentially quantitative yield in...

Descripción completa

Detalles Bibliográficos
Autores principales: Neal, Edward A., Goldup, Stephen M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645920/
https://www.ncbi.nlm.nih.gov/pubmed/29308153
http://dx.doi.org/10.1039/c4sc03999h
_version_ 1783271982120304640
author Neal, Edward A.
Goldup, Stephen M.
author_facet Neal, Edward A.
Goldup, Stephen M.
author_sort Neal, Edward A.
collection PubMed
description We recently identified competitive formation of doubly interlocked [3]rotaxanes as the origin of the non-linear variation in yield of [2]rotaxane with macrocycle size in the bipyridine-mediated AT-CuAAC reaction. Selection of reaction conditions gave [2]rotaxanes in essentially quantitative yield in all cases and hard to access doubly threaded [3]rotaxanes in up to 50% yield in a single, four component coupling. Based on the effect of macrocycle structure on the reaction outcome we propose a detailed mechanism of [3]rotaxane formation.
format Online
Article
Text
id pubmed-5645920
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-56459202018-01-05 Competitive formation of homocircuit [3]rotaxanes in synthetically useful yields in the bipyridine-mediated active template CuAAC reaction Neal, Edward A. Goldup, Stephen M. Chem Sci Chemistry We recently identified competitive formation of doubly interlocked [3]rotaxanes as the origin of the non-linear variation in yield of [2]rotaxane with macrocycle size in the bipyridine-mediated AT-CuAAC reaction. Selection of reaction conditions gave [2]rotaxanes in essentially quantitative yield in all cases and hard to access doubly threaded [3]rotaxanes in up to 50% yield in a single, four component coupling. Based on the effect of macrocycle structure on the reaction outcome we propose a detailed mechanism of [3]rotaxane formation. Royal Society of Chemistry 2015-04-01 2015-02-03 /pmc/articles/PMC5645920/ /pubmed/29308153 http://dx.doi.org/10.1039/c4sc03999h Text en This journal is © The Royal Society of Chemistry 2015 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Neal, Edward A.
Goldup, Stephen M.
Competitive formation of homocircuit [3]rotaxanes in synthetically useful yields in the bipyridine-mediated active template CuAAC reaction
title Competitive formation of homocircuit [3]rotaxanes in synthetically useful yields in the bipyridine-mediated active template CuAAC reaction
title_full Competitive formation of homocircuit [3]rotaxanes in synthetically useful yields in the bipyridine-mediated active template CuAAC reaction
title_fullStr Competitive formation of homocircuit [3]rotaxanes in synthetically useful yields in the bipyridine-mediated active template CuAAC reaction
title_full_unstemmed Competitive formation of homocircuit [3]rotaxanes in synthetically useful yields in the bipyridine-mediated active template CuAAC reaction
title_short Competitive formation of homocircuit [3]rotaxanes in synthetically useful yields in the bipyridine-mediated active template CuAAC reaction
title_sort competitive formation of homocircuit [3]rotaxanes in synthetically useful yields in the bipyridine-mediated active template cuaac reaction
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645920/
https://www.ncbi.nlm.nih.gov/pubmed/29308153
http://dx.doi.org/10.1039/c4sc03999h
work_keys_str_mv AT nealedwarda competitiveformationofhomocircuit3rotaxanesinsyntheticallyusefulyieldsinthebipyridinemediatedactivetemplatecuaacreaction
AT goldupstephenm competitiveformationofhomocircuit3rotaxanesinsyntheticallyusefulyieldsinthebipyridinemediatedactivetemplatecuaacreaction