Please use this identifier to cite or link to this item:
https://hdl.handle.net/1959.11/5139| Title: | 'N'-Heteroatom-substituted hydroxamic esters | Contributor(s): | Glover, Stephen (author) |
Publication Date: | 2009 | Handle Link: | https://hdl.handle.net/1959.11/5139 | Abstract: | The properties of amides are determinants of the structure and characteristics of a wide range of molecules and particularly those of peptides and proteins. Hydroxamic esters, as a subset of the amide functionality, possess many structural features in common with the more abundant linkage. Amide linkages in hydroxamic esters and amides are characterized by a nitrogen that is essentially sp² hybridized and a lone pair that resides in a 2pz orbital. | Publication Type: | Book Chapter | Source of Publication: | The Chemistry of Hydroxylamines, Oximes and Hydroxamic Acids, v.1, p. 839-923 | Publisher: | John Wiley & Sons Ltd | Place of Publication: | Chichester, United Kingdom | ISBN: | 047051261X 9780470512616 |
Fields of Research (FoR) 2008: | 030505 Physical Organic Chemistry 030799 Theoretical and Computational Chemistry not elsewhere classified 030503 Organic Chemical Synthesis |
Socio-Economic Objective (SEO) 2008: | 970103 Expanding Knowledge in the Chemical Sciences | HERDC Category Description: | B1 Chapter in a Scholarly Book | Publisher/associated links: | http://books.google.com.au/books?id=XKP-mFbCs_0C&lpg=PP1&pg=PA839 http://au.wiley.com/WileyCDA/WileyTitle/productCd-047051261X,descCd-description.html http://nla.gov.au/anbd.bib-an43770197 |
Series Name: | Patai Series: Functional Groups in Organic Chemistry | Editor: | Editor(s): Zvi Rappoport and Joel Liebman |
|---|---|
| Appears in Collections: | Book Chapter School of Science and Technology |
Files in This Item:
| File | Description | Size | Format |
|---|
Page view(s)
1,116
checked on Mar 9, 2023
Items in Research UNE are protected by copyright, with all rights reserved, unless otherwise indicated.