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https://hdl.handle.net/1959.11/5139
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DC Field | Value | Language |
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dc.contributor.author | Glover, Stephen | en |
local.source.editor | Editor(s): Zvi Rappoport and Joel Liebman | en |
dc.date.accessioned | 2010-03-16T12:26:00Z | - |
dc.date.issued | 2009 | - |
dc.identifier.citation | The Chemistry of Hydroxylamines, Oximes and Hydroxamic Acids, v.1, p. 839-923 | en |
dc.identifier.isbn | 047051261X | en |
dc.identifier.isbn | 9780470512616 | en |
dc.identifier.uri | https://hdl.handle.net/1959.11/5139 | - |
dc.description.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. | en |
dc.language | en | en |
dc.publisher | John Wiley & Sons Ltd | en |
dc.relation.ispartof | The Chemistry of Hydroxylamines, Oximes and Hydroxamic Acids | en |
dc.relation.ispartofseries | Patai Series: Functional Groups in Organic Chemistry | en |
dc.relation.isversionof | 1 | en |
dc.title | 'N'-Heteroatom-substituted hydroxamic esters | en |
dc.type | Book Chapter | en |
dc.subject.keywords | Organic Chemical Synthesis | en |
dc.subject.keywords | Theoretical and Computational Chemistry | en |
dc.subject.keywords | Physical Organic Chemistry | en |
local.contributor.firstname | Stephen | en |
local.subject.for2008 | 030505 Physical Organic Chemistry | en |
local.subject.for2008 | 030799 Theoretical and Computational Chemistry not elsewhere classified | en |
local.subject.for2008 | 030503 Organic Chemical Synthesis | en |
local.subject.seo2008 | 970103 Expanding Knowledge in the Chemical Sciences | en |
local.profile.school | School of Science and Technology | en |
local.profile.email | sglover@une.edu.au | en |
local.output.category | B1 | en |
local.record.place | au | en |
local.record.institution | University of New England | en |
local.identifier.epublicationsrecord | une-20090813-135123 | en |
local.publisher.place | Chichester, United Kingdom | en |
local.identifier.totalchapters | 18 | en |
local.format.startpage | 839 | en |
local.format.endpage | 923 | en |
local.identifier.volume | 1 | en |
local.contributor.lastname | Glover | en |
dc.identifier.staff | une-id:sglover | en |
local.profile.orcid | 0000-0002-9344-8669 | en |
local.profile.role | author | en |
local.identifier.unepublicationid | une:5257 | en |
dc.identifier.academiclevel | Academic | en |
local.title.maintitle | 'N'-Heteroatom-substituted hydroxamic esters | en |
local.output.categorydescription | B1 Chapter in a Scholarly Book | en |
local.relation.url | http://books.google.com.au/books?id=XKP-mFbCs_0C&lpg=PP1&pg=PA839 | en |
local.relation.url | http://au.wiley.com/WileyCDA/WileyTitle/productCd-047051261X,descCd-description.html | en |
local.relation.url | http://nla.gov.au/anbd.bib-an43770197 | en |
local.search.author | Glover, Stephen | en |
local.uneassociation | Unknown | en |
local.year.published | 2009 | en |
Appears in Collections: | Book Chapter School of Science and Technology |
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