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Facile reduction of coordinated α-imino acids to amino acids by dithionite and borohydride.

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dc.contributor.authorPearce, Dierdre
dc.contributor.authorHartshorn, Richard
dc.contributor.authorSargeson, Alan
dc.date.accessioned2015-12-13T22:23:01Z
dc.date.available2015-12-13T22:23:01Z
dc.date.issued2002
dc.date.updated2015-12-11T08:02:03Z
dc.description.abstractSodium dithionite was found to reduce a range of α-iminoacidato ligands, chelated to cobalt(III), to the related α-aminoacidato species. For the bis(1,2-ethanediamine) system, the distribution of the products showed a small stereoselectivity towards the
dc.identifier.issn1477-9226
dc.identifier.urihttp://hdl.handle.net/1885/72565
dc.publisherRoyal Society of Chemistry
dc.sourceDalton Transactions
dc.subjectKeywords: Chelation; Molecules; pH effects; Reduction; Imino acids; Amino acids
dc.titleFacile reduction of coordinated α-imino acids to amino acids by dithionite and borohydride.
dc.typeJournal article
local.bibliographicCitation.lastpage1752
local.bibliographicCitation.startpage1747
local.contributor.affiliationPearce, Dierdre, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationHartshorn, Richard, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationSargeson, Alan, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidPearce, Dierdre, u3768328
local.contributor.authoruidHartshorn, Richard, u3688532
local.contributor.authoruidSargeson, Alan, u5800192
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationMigratedxPub3309
local.identifier.scopusID2-s2.0-0036009975
local.type.statusPublished Version

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