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a-Benzoyloxy- and a-methoxy-substituted glycine derivatives as atypical substrates for free-radical reactions with stannanes

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dc.contributor.authorEaston, Christopher
dc.contributor.authorPeters, Steven C
dc.date.accessioned2015-12-13T23:35:09Z
dc.date.available2015-12-13T23:35:09Z
dc.date.issued1999
dc.date.updated2015-12-12T09:38:51Z
dc.description.abstractα-Benzoyloxy-and α-methoxy-substituted glycine derivatives undergo homolytic reactions with tributyltin hydride to give the reduction product. With allyltributyltin they afford the product of allyl group transfer and the corresponding dimeric glycine de
dc.identifier.issn1042-6507
dc.identifier.urihttp://hdl.handle.net/1885/93777
dc.publisherGordon and Breach
dc.sourcePhosphorus, Sulfur, and Silicon and the Related Elements
dc.subjectKeywords: Allyltributyltin; Benzoate; Free-radical; Hexabutylditin; Methoxide; Tributyltin hydride
dc.titlea-Benzoyloxy- and a-methoxy-substituted glycine derivatives as atypical substrates for free-radical reactions with stannanes
dc.typeJournal article
local.bibliographicCitation.lastpage166
local.bibliographicCitation.startpage57
local.contributor.affiliationEaston, Christopher, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationPeters, Steven C, University of Adelaide
local.contributor.authoruidEaston, Christopher, u9500570
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationMigratedxPub25183
local.identifier.citationvolume150-151
local.identifier.scopusID2-s2.0-4243748152
local.type.statusPublished Version

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