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

Easton, Christopher; Peters, Steven C

Description

α-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.contributor.authorEaston, Christopher
dc.contributor.authorPeters, Steven C
dc.date.accessioned2015-12-13T23:35:09Z
dc.date.available2015-12-13T23:35:09Z
dc.identifier.issn1042-6507
dc.identifier.urihttp://hdl.handle.net/1885/93777
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.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.description.notesImported from ARIES
local.description.refereedYes
local.identifier.citationvolume150-151
dc.date.issued1999
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationMigratedxPub25183
local.type.statusPublished Version
local.contributor.affiliationEaston, Christopher, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationPeters, Steven C, University of Adelaide
local.bibliographicCitation.startpage57
local.bibliographicCitation.lastpage166
dc.date.updated2015-12-12T09:38:51Z
local.identifier.scopusID2-s2.0-4243748152
CollectionsANU Research Publications

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