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The synthesis of a pyridine-: N -oxide isophthalamide rotaxane utilizing supplementary amide hydrogen bond interactions

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The synthesis of a pyridine-: N -oxide isophthalamide rotaxane utilizing supplementary amide hydrogen bond interactions. / Evans, Nicholas Henley; Gell, Charlie; Peach, Michael Joseph George.
In: Organic and Biomolecular Chemistry , Vol. 14, No. 33, 07.09.2016, p. 7972-7981.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

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Evans NH, Gell C, Peach MJG. The synthesis of a pyridine-: N -oxide isophthalamide rotaxane utilizing supplementary amide hydrogen bond interactions. Organic and Biomolecular Chemistry . 2016 Sept 7;14(33):7972-7981. Epub 2016 Aug 1. doi: 10.1039/C6OB01435F

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@article{dc83ffe627a2462abdc0ead2432a3601,
title = "The synthesis of a pyridine-: N -oxide isophthalamide rotaxane utilizing supplementary amide hydrogen bond interactions",
abstract = "The synthesis of a pyridine-N-oxide containing rotaxane, not requiring an additional ionic template, has been achieved in 32% yield. Successful rotaxane formation is dependent upon the structure of the isophthalamide macrocycle used, an observation which has been rationalised by a combination of NMR spectroscopy, X-ray crystallography and computational modelling.",
author = "Evans, {Nicholas Henley} and Charlie Gell and Peach, {Michael Joseph George}",
note = "{\textcopyright} Royal Society of Chemistry 2016",
year = "2016",
month = sep,
day = "7",
doi = "10.1039/C6OB01435F",
language = "English",
volume = "14",
pages = "7972--7981",
journal = "Organic and Biomolecular Chemistry ",
issn = "1477-0520",
publisher = "Royal Society of Chemistry",
number = "33",

}

RIS

TY - JOUR

T1 - The synthesis of a pyridine-: N -oxide isophthalamide rotaxane utilizing supplementary amide hydrogen bond interactions

AU - Evans, Nicholas Henley

AU - Gell, Charlie

AU - Peach, Michael Joseph George

N1 - © Royal Society of Chemistry 2016

PY - 2016/9/7

Y1 - 2016/9/7

N2 - The synthesis of a pyridine-N-oxide containing rotaxane, not requiring an additional ionic template, has been achieved in 32% yield. Successful rotaxane formation is dependent upon the structure of the isophthalamide macrocycle used, an observation which has been rationalised by a combination of NMR spectroscopy, X-ray crystallography and computational modelling.

AB - The synthesis of a pyridine-N-oxide containing rotaxane, not requiring an additional ionic template, has been achieved in 32% yield. Successful rotaxane formation is dependent upon the structure of the isophthalamide macrocycle used, an observation which has been rationalised by a combination of NMR spectroscopy, X-ray crystallography and computational modelling.

U2 - 10.1039/C6OB01435F

DO - 10.1039/C6OB01435F

M3 - Journal article

VL - 14

SP - 7972

EP - 7981

JO - Organic and Biomolecular Chemistry

JF - Organic and Biomolecular Chemistry

SN - 1477-0520

IS - 33

ER -