C-18 Hydroxylation of gibberellins

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dc.contributor.authorMander, Lewis
dc.contributor.authorThomson, Regan
dc.date.accessioned2015-12-13T23:16:15Z
dc.date.available2015-12-13T23:16:15Z
dc.date.issued2000
dc.date.updated2015-12-12T08:47:17Z
dc.description.abstractA protocol for the hydroxylation of the 18-methyl group in gibberellins has been developed, as demonstrated by the successful synthesis of 18-hydroxy GA4 methyl ester by means of a tandem process involving the conjugate addition of alkoxide to the α-meth
dc.identifier.issn1470-4358
dc.identifier.urihttp://hdl.handle.net/1885/89310
dc.publisherRoyal Society of Chemistry
dc.sourceJournal of the Chemical Society, Perkin Transactions 1
dc.subjectKeywords: Addition reactions; Chemical bonds; Derivatives; Hydroxylation; Isomers; Nuclear magnetic resonance spectroscopy; Synthesis (chemical); Gibberellins; Esters
dc.titleC-18 Hydroxylation of gibberellins
dc.typeJournal article
local.bibliographicCitation.lastpage2894
local.bibliographicCitation.startpage2893
local.contributor.affiliationMander, Lewis, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationThomson, Regan, College of Physical and Mathematical Sciences, ANU
local.contributor.authoremailu7500768@anu.edu.au
local.contributor.authoruidMander, Lewis, u7500768
local.contributor.authoruidThomson, Regan, u9718127
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor030499 - Medicinal and Biomolecular Chemistry not elsewhere classified
local.identifier.ariespublicationMigratedxPub19285
local.identifier.citationvolume17
local.identifier.doi10.1039/b006044p
local.identifier.scopusID2-s2.0-0034618933
local.identifier.uidSubmittedByMigrated
local.type.statusPublished Version

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