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Synthesis of the β-hydroxydopa-γ-hydroxy-δ-sulfinylnorvaline component of ustiloxins A and B

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dc.contributor.authorHunter, Luke
dc.contributor.authorMcLeod, Malcolm
dc.contributor.authorHutton, Craig A
dc.date.accessioned2015-12-10T22:23:59Z
dc.date.issued2005
dc.date.updated2015-12-09T09:12:55Z
dc.description.abstractThe dopa-sulfinylnorvaline component of ustiloxins A and B has been prepared using an Evans salen-Al-catalysed aldol reaction with a 6-mercaptoisovanillin derivative, followed by incorporation of the norvaline group and asymmetric oxidation of the resulting sulfide to give the corresponding sulfoxide.
dc.identifier.issn1477-0520
dc.identifier.urihttp://hdl.handle.net/1885/53057
dc.publisherRoyal Society of Chemistry
dc.sourceOrganic and Biomolecular Chemistry
dc.subjectKeywords: Alcohols; Alkylation; Aluminum compounds; Catalysis; Chemical modification; Isomers; Oxidation; Reaction kinetics; Sulfur compounds; Synthesis (chemical); Antimitotic agents; Steroselectivity; Sulfinylinorvaline synthesis; Sulfoxides; Aromatic compounds;
dc.titleSynthesis of the β-hydroxydopa-γ-hydroxy-δ-sulfinylnorvaline component of ustiloxins A and B
dc.typeJournal article
local.bibliographicCitation.issue5
local.bibliographicCitation.lastpage734
local.bibliographicCitation.startpage732
local.contributor.affiliationHunter, Luke, University of Sydney
local.contributor.affiliationMcLeod, Malcolm, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationHutton, Craig A, University of Melbourne
local.contributor.authoruidMcLeod, Malcolm, u4045340
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationu4005981xPUB263
local.identifier.citationvolume3
local.identifier.doi10.1039/b418876d
local.identifier.scopusID2-s2.0-15244350598
local.type.statusPublished Version

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