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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.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.type.statusPublished Version

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