Rapid, Chemoenzymatic Syntheses of the Epoxyquinols (−)-Bromoxone Acetate and (−)-Tricholomenyn A

dc.contributor.authorPinkerton, David
dc.contributor.authorBanwell, Martin
dc.contributor.authorWillis, Anthony
dc.date.accessioned2015-12-07T22:23:09Z
dc.date.issued2009
dc.date.updated2016-02-24T09:51:21Z
dc.description.abstractThe epoxyquinol derivatives (-)-bromoxone acetate (ent-1) and (-)-tricholomenyn A (2) have been prepared from the cis-1,2-dihydrocatechols 3 and 4, respectively. Compounds 3 and 4 are themselves obtained in enantiomerically pure form through the whole-cell biotransformation of the corresponding halobenzene.
dc.identifier.issn0004-9425
dc.identifier.urihttp://hdl.handle.net/1885/20536
dc.publisherCSIRO Publishing
dc.sourceAustralian Journal of Chemistry
dc.subjectKeywords: Chemo-enzymatic synthesis; Epoxyquinol; Whole-cell biotransformations
dc.titleRapid, Chemoenzymatic Syntheses of the Epoxyquinols (−)-Bromoxone Acetate and (−)-Tricholomenyn A
dc.typeJournal article
local.bibliographicCitation.issue12
local.bibliographicCitation.lastpage1645
local.bibliographicCitation.startpage1639
local.contributor.affiliationPinkerton, David, 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.authoruidPinkerton, David, u3968575
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.ariespublicationu2544221xPUB13
local.identifier.citationvolume62
local.identifier.doi10.1071/CH09469
local.identifier.scopusID2-s2.0-76849105736
local.identifier.thomsonID000272597300010
local.identifier.uidSubmittedByu2544221
local.type.statusPublished Version

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