Home > Research > Publications & Outputs > Catalytically generated N-acyliminium ions and ...

Electronic data

  • 2022OwenMRes

    Final published version, 4 MB, PDF document

    Available under license: None

Text available via DOI:

View graph of relations

Catalytically generated N-acyliminium ions and their application in Diels-Alder reactions.

Research output: ThesisMaster's Thesis

Published

Standard

Catalytically generated N-acyliminium ions and their application in Diels-Alder reactions. / Owen, Niamh.
Lancaster University, 2022. 131 p.

Research output: ThesisMaster's Thesis

Harvard

APA

Vancouver

Owen N. Catalytically generated N-acyliminium ions and their application in Diels-Alder reactions.. Lancaster University, 2022. 131 p. doi: 10.17635/lancaster/thesis/1808

Author

Bibtex

@mastersthesis{fdfec231add74a76a9de6cfa5c5455a6,
title = "Catalytically generated N-acyliminium ions and their application in Diels-Alder reactions.",
abstract = "Society is currently facing major challenges in providing resources such as healthcare in a more sustainable manner. The production of pharmaceuticals relies heavily on the use of precious transition metals such as palladium and rhodium to mediate single transformations on route to desired bioactive substances. Although these transformations are often high yielding, the need to mine great quantities of these metals remains a concern. Therefore, synthetic chemists must strive to develop more environmentally friendly and sustainable chemistry to access desirable and important scaffolds.We report on the development of a novel route to tricyclic lactam products via a facile Aza-Diels-Alder reaction of catalytically generated N-acyliminium ions. Employing a Ca(NTf2)2 / nBu4NPF6 catalyst system in low loadings, to synthesise a diverse range of fused ring systems which differing electronic and steric properties in predominately good yields.",
author = "Niamh Owen",
year = "2022",
month = oct,
day = "24",
doi = "10.17635/lancaster/thesis/1808",
language = "English",
publisher = "Lancaster University",
school = "Chemistry",

}

RIS

TY - THES

T1 - Catalytically generated N-acyliminium ions and their application in Diels-Alder reactions.

AU - Owen, Niamh

PY - 2022/10/24

Y1 - 2022/10/24

N2 - Society is currently facing major challenges in providing resources such as healthcare in a more sustainable manner. The production of pharmaceuticals relies heavily on the use of precious transition metals such as palladium and rhodium to mediate single transformations on route to desired bioactive substances. Although these transformations are often high yielding, the need to mine great quantities of these metals remains a concern. Therefore, synthetic chemists must strive to develop more environmentally friendly and sustainable chemistry to access desirable and important scaffolds.We report on the development of a novel route to tricyclic lactam products via a facile Aza-Diels-Alder reaction of catalytically generated N-acyliminium ions. Employing a Ca(NTf2)2 / nBu4NPF6 catalyst system in low loadings, to synthesise a diverse range of fused ring systems which differing electronic and steric properties in predominately good yields.

AB - Society is currently facing major challenges in providing resources such as healthcare in a more sustainable manner. The production of pharmaceuticals relies heavily on the use of precious transition metals such as palladium and rhodium to mediate single transformations on route to desired bioactive substances. Although these transformations are often high yielding, the need to mine great quantities of these metals remains a concern. Therefore, synthetic chemists must strive to develop more environmentally friendly and sustainable chemistry to access desirable and important scaffolds.We report on the development of a novel route to tricyclic lactam products via a facile Aza-Diels-Alder reaction of catalytically generated N-acyliminium ions. Employing a Ca(NTf2)2 / nBu4NPF6 catalyst system in low loadings, to synthesise a diverse range of fused ring systems which differing electronic and steric properties in predominately good yields.

U2 - 10.17635/lancaster/thesis/1808

DO - 10.17635/lancaster/thesis/1808

M3 - Master's Thesis

PB - Lancaster University

ER -