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The domino intramolecular Diels-Alder approach to 16-oxasteroids

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dc.contributor.authorTurner, Craigen_AU
dc.contributor.authorWilliamson, Rachelen_AU
dc.contributor.authorTurner, Peteren_AU
dc.contributor.authorSherburn, Michaelen_AU
dc.date.accessioned2015-12-13T23:06:02Z
dc.date.issued2003
dc.date.updated2015-12-12T08:03:25Z
dc.description.abstractThis communication describes the use of the zipper mode domino IMDA strategy for the one step construction of enantiomerically pure steroid-type frameworks.
dc.identifier.issn1359-7345
dc.identifier.urihttp://hdl.handle.net/1885/85833
dc.publisherRoyal Society of Chemistry
dc.sourceChemical Communications
dc.subjectKeywords: 16 oxasteroid derivative; steroid; unclassified drug; article; chemical reaction; chemical structure; complex formation; covalent bond; cycloaddition; Diels Alder reaction; enantiomer; molecular stability; stereochemistry
dc.titleThe domino intramolecular Diels-Alder approach to 16-oxasteroids
dc.typeJournal article
local.bibliographicCitation.issue13
local.bibliographicCitation.lastpage1611
local.bibliographicCitation.startpage1610
local.contributor.affiliationTurner, Craig, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationWilliamson, Rachel, Massey University
local.contributor.affiliationTurner, Peter, University of Sydney
local.contributor.affiliationSherburn, Michael, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidTurner, Craig, u4054591
local.contributor.authoruidSherburn, Michael, u4053118
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationMigratedxPub14497
local.identifier.doi10.1039/b303362g
local.identifier.scopusID2-s2.0-0038818553
local.type.statusPublished Version

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