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https://hdl.handle.net/1959.11/20612
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Wilkinson, Brendan | en |
dc.date.accessioned | 2017-05-02T12:23:00Z | - |
dc.date.issued | 2013 | - |
dc.identifier.citation | Australian Journal of Chemistry, 66(8), p. 910-912 | en |
dc.identifier.issn | 1445-0038 | en |
dc.identifier.issn | 0004-9425 | en |
dc.identifier.uri | https://hdl.handle.net/1959.11/20612 | - |
dc.description.abstract | Acylated derivatives of 1-hydroxybenzotriazole (HOBt) have been widely used as reactive intermediates in a variety of one-pot, bond forming reactions. Isolable benzotriazole 'esters' 1-(benzoyloxy)benzotriazole (1-BBTZ, 1) and 1-(acetoxy)benzotriazole (2) are also useful reagents for the regioselective acylation of diols and partially protected carbohydrates (Fig. 1).[¹] 1-(Acyloxy) benzotriazoles 1 and 2 can be conveniently prepared by a carbodiimide-promoted condensation of HOBt,[²] or via the corresponding acyl chloride.[¹] | en |
dc.language | en | en |
dc.publisher | CSIRO Publishing | en |
dc.relation.ispartof | Australian Journal of Chemistry | en |
dc.title | 1-(Acyloxy)benzotriazoles: Useful Reagents for the Regioselective Acylation of Diols | en |
dc.type | Journal Article | en |
dc.identifier.doi | 10.1071/ch13303 | en |
dc.subject.keywords | Organic Chemical Synthesis | en |
dc.subject.keywords | Organic Chemistry | en |
dc.subject.keywords | Biologically Active Molecules | en |
local.contributor.firstname | Brendan | en |
local.subject.for2008 | 030401 Biologically Active Molecules | en |
local.subject.for2008 | 030503 Organic Chemical Synthesis | en |
local.subject.for2008 | 030599 Organic Chemistry not elsewhere classified | en |
local.subject.seo2008 | 970103 Expanding Knowledge in the Chemical Sciences | en |
local.subject.seo2008 | 929999 Health not elsewhere classified | en |
local.profile.school | School of Science and Technology | en |
local.profile.email | bwilkin7@une.edu.au | en |
local.output.category | C1 | en |
local.record.place | au | en |
local.record.institution | University of New England | en |
local.identifier.epublicationsrecord | une-20170323-114921 | en |
local.publisher.place | Australia | en |
local.format.startpage | 910 | en |
local.format.endpage | 912 | en |
local.identifier.scopusid | 84882597040 | en |
local.peerreviewed | Yes | en |
local.identifier.volume | 66 | en |
local.identifier.issue | 8 | en |
local.title.subtitle | Useful Reagents for the Regioselective Acylation of Diols | en |
local.contributor.lastname | Wilkinson | en |
dc.identifier.staff | une-id:bwilkin7 | en |
local.profile.orcid | 0000-0003-1866-6540 | en |
local.profile.role | author | en |
local.identifier.unepublicationid | une:20804 | en |
dc.identifier.academiclevel | Academic | en |
local.title.maintitle | 1-(Acyloxy)benzotriazoles | en |
local.output.categorydescription | C1 Refereed Article in a Scholarly Journal | en |
local.relation.grantdescription | ARC/DE130101673 | en |
local.search.author | Wilkinson, Brendan | en |
local.uneassociation | Unknown | en |
local.year.published | 2013 | en |
local.subject.for2020 | 340401 Biologically active molecules | en |
local.subject.for2020 | 340503 Organic chemical synthesis | en |
local.subject.seo2020 | 280105 Expanding knowledge in the chemical sciences | en |
local.codeupdate.date | 2022-02-08T15:38:49.171 | en |
local.codeupdate.eperson | bwilkin7@une.edu.au | en |
local.codeupdate.finalised | true | en |
local.original.for2020 | undefined | en |
local.original.for2020 | 340503 Organic chemical synthesis | en |
local.original.for2020 | 340401 Biologically active molecules | en |
local.original.seo2020 | 280105 Expanding knowledge in the chemical sciences | en |
local.original.seo2020 | undefined | en |
Appears in Collections: | Journal Article School of Science and Technology |
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