dc.contributor.author |
Itumoh, Emeka J |
|
dc.contributor.author |
Data, Shailja |
|
dc.contributor.author |
Leitao, Erin M |
|
dc.coverage.spatial |
Switzerland |
|
dc.date.accessioned |
2023-03-15T23:23:24Z |
|
dc.date.available |
2023-03-15T23:23:24Z |
|
dc.date.issued |
2020-08 |
|
dc.identifier.citation |
(2020). Molecules, 25(16), E3684-. |
|
dc.identifier.issn |
1420-3049 |
|
dc.identifier.uri |
https://hdl.handle.net/2292/63390 |
|
dc.description.abstract |
This review covers the main synthetic routes to and the corresponding mechanisms of phosphoramidate formation. The synthetic routes can be separated into six categories: salt elimination, oxidative cross-coupling, azide, reduction, hydrophosphinylation, and phosphoramidate-aldehyde-dienophile (PAD). Examples of some important compounds synthesized through these routes are provided. As an important class of organophosphorus compounds, the applications of phosphoramidate compounds, are also briefly introduced. |
|
dc.format.medium |
Electronic |
|
dc.language |
eng |
|
dc.publisher |
MDPI |
|
dc.relation.ispartofseries |
Molecules (Basel, Switzerland) |
|
dc.rights |
Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. |
|
dc.rights.uri |
https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm |
|
dc.rights.uri |
https://creativecommons.org/licenses/by/4.0/ |
|
dc.subject |
Phosphoric Acids |
|
dc.subject |
Amides |
|
dc.subject |
Chemistry Techniques, Synthetic |
|
dc.subject |
applications |
|
dc.subject |
mechanism |
|
dc.subject |
phosphoramidate |
|
dc.subject |
synthetic routes |
|
dc.subject |
Science & Technology |
|
dc.subject |
Life Sciences & Biomedicine |
|
dc.subject |
Physical Sciences |
|
dc.subject |
Biochemistry & Molecular Biology |
|
dc.subject |
Chemistry, Multidisciplinary |
|
dc.subject |
Chemistry |
|
dc.subject |
POLYPHOSPHORAMIDATE GENE CARRIERS |
|
dc.subject |
AMMONO PHOSPHORIC-ACIDS |
|
dc.subject |
ATHERTON-TODD REACTION |
|
dc.subject |
ONE-POT SYNTHESIS |
|
dc.subject |
CATALYZED PHOSPHORAMIDATION |
|
dc.subject |
BIOLOGICAL EVALUATION |
|
dc.subject |
INSECTICIDAL ACTIVITY |
|
dc.subject |
UREASE INHIBITORS |
|
dc.subject |
FLAME RETARDANTS |
|
dc.subject |
H-PHOSPHONATES |
|
dc.subject |
0304 Medicinal and Biomolecular Chemistry |
|
dc.subject |
0305 Organic Chemistry |
|
dc.subject |
0307 Theoretical and Computational Chemistry |
|
dc.title |
Opening up the Toolbox: Synthesis and Mechanisms of Phosphoramidates. |
|
dc.type |
Journal Article |
|
dc.identifier.doi |
10.3390/molecules25163684 |
|
pubs.issue |
16 |
|
pubs.begin-page |
E3684 |
|
pubs.volume |
25 |
|
dc.date.updated |
2023-02-28T19:24:59Z |
|
dc.rights.holder |
Copyright: The authors |
en |
dc.identifier.pmid |
32823507 (pubmed) |
|
pubs.author-url |
https://www.ncbi.nlm.nih.gov/pubmed/32823507 |
|
pubs.publication-status |
Published |
|
dc.rights.accessrights |
http://purl.org/eprint/accessRights/OpenAccess |
en |
pubs.subtype |
IM |
|
pubs.subtype |
review-article |
|
pubs.subtype |
Review |
|
pubs.subtype |
Journal Article |
|
pubs.elements-id |
824423 |
|
dc.identifier.eissn |
1420-3049 |
|
dc.identifier.pii |
molecules25163684 |
|
pubs.number |
ARTN 3684 |
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pubs.record-created-at-source-date |
2023-03-01 |
|
pubs.online-publication-date |
2020-08-13 |
|