Intramolecular cycloaddition reactions of cis-1,2-dihydrocatechol derivatives incorporating C3 tethered diazoketones, nitrile oxides and azides: stereocontrolled routes to enantiomerically pure spiro[5.5]undecanes and related systems

dc.contributor.authorReekie, Tristan
dc.contributor.authorBanwell, Martin
dc.contributor.authorWillis, Anthony
dc.date.accessioned2015-12-10T23:03:17Z
dc.date.issued2013
dc.date.updated2016-02-24T10:25:40Z
dc.description.abstractA series of enantiomerically pure cis-1,2-dihydrocatechol derivatives incorporating C3-tethered diazoketone, nitrile oxide, or azide residues has been prepared from the precursor iodide 7 using Negishi cross-coupling reactions. Such derivatives, including
dc.identifier.issn0022-3263
dc.identifier.urihttp://hdl.handle.net/1885/62109
dc.publisherAmerican Chemical Society
dc.sourceJournal of Organic Chemistry
dc.subjectKeywords: Diazoketones; Intramolecular cycloaddition reactions; Negishi cross-coupling; Nitrile oxides; Related systems; Stereo-selective; Cycloaddition; Nitrogen oxides; Enantiomers; azide; catechol derivative; fused alicyclic compound; ketone derivative; nitrile
dc.titleIntramolecular cycloaddition reactions of cis-1,2-dihydrocatechol derivatives incorporating C3 tethered diazoketones, nitrile oxides and azides: stereocontrolled routes to enantiomerically pure spiro[5.5]undecanes and related systems
dc.typeJournal article
local.bibliographicCitation.issue14
local.bibliographicCitation.lastpage7111
local.bibliographicCitation.startpage7100
local.contributor.affiliationReekie, Tristan, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationBanwell, Martin, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationWillis, Anthony, College of Physical and Mathematical Sciences, ANU
local.contributor.authoremailu9500594@anu.edu.au
local.contributor.authoruidReekie, Tristan, u2566255
local.contributor.authoruidBanwell, Martin, u9500594
local.contributor.authoruidWillis, Anthony, u8512028
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.absseo970103 - Expanding Knowledge in the Chemical Sciences
local.identifier.ariespublicationu4005981xPUB669
local.identifier.citationvolume78
local.identifier.doi10.1021/jo400952u
local.identifier.scopusID2-s2.0-84880535743
local.identifier.thomsonID000322210700026
local.identifier.uidSubmittedByu4005981
local.type.statusPublished Version

Downloads

Original bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
01_Reekie_Intramolecular_cycloaddition_2013.pdf
Size:
482.58 KB
Format:
Adobe Portable Document Format