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cis-1,2-Dihydrocatechols in chemical synthesis: first synthesis of L-ascorbic acid (vitamin C) from a non-carbohydrate source

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dc.contributor.authorBanwell, Martin
dc.contributor.authorBlakey, Simon
dc.contributor.authorHarfoot, Gwion
dc.contributor.authorLongmore, Robert
dc.date.accessioned2015-12-13T23:35:05Z
dc.date.available2015-12-13T23:35:05Z
dc.date.issued1999
dc.date.updated2015-12-12T09:38:37Z
dc.description.abstractThe cis-1,2-dihydrocatechol (2), which is obtained in enantiopure form by microbial oxidation of chlorobenzene, has been converted, via 3,5-O-benzylidene-L-gulono-1,4-lactone (8), into L-ascorbic acid (1).
dc.identifier.issn0004-9425
dc.identifier.urihttp://hdl.handle.net/1885/93744
dc.publisherCSIRO Publishing
dc.sourceAustralian Journal of Chemistry
dc.titlecis-1,2-Dihydrocatechols in chemical synthesis: first synthesis of L-ascorbic acid (vitamin C) from a non-carbohydrate source
dc.typeJournal article
local.bibliographicCitation.lastpage142
local.bibliographicCitation.startpage137
local.contributor.affiliationBanwell, Martin, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationBlakey, Simon, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationHarfoot, Gwion, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationLongmore, Robert, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidBanwell, Martin, u9500594
local.contributor.authoruidBlakey, Simon, u961687
local.contributor.authoruidHarfoot, Gwion, u9717909
local.contributor.authoruidLongmore, Robert, u1556935
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationMigratedxPub25143
local.identifier.citationvolume52
local.identifier.scopusID2-s2.0-0000495312
local.type.statusPublished Version

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