Studies toward the total synthesis of nominine

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dc.contributor.authorHutt, Oliver
dc.contributor.authorMander, Lewis
dc.date.accessioned2015-12-10T21:56:54Z
dc.date.issued2007
dc.date.updated2015-12-09T07:41:56Z
dc.description.abstract(Chemical Equation Presented) The construction of the hetisane group of alkaloids, of which the extensively bridged nominine 17 is the simplest member, poses the ultimate challenge for those interested in the synthesis of the C 20 diterpene alkaloids. We
dc.identifier.issn0022-3263
dc.identifier.urihttp://hdl.handle.net/1885/39656
dc.publisherAmerican Chemical Society
dc.sourceJournal of Organic Chemistry
dc.subjectKeywords: Birch reduction; Lewis acid; Reductive acylation; Acylation; Catalysis; Molecular interactions; Reaction kinetics; Synthesis (chemical); Organic compounds; alkaloid derivative; carbamic acid; diterpene; Lewis acid; nominine; unclassified drug; acylation;
dc.titleStudies toward the total synthesis of nominine
dc.typeJournal article
local.bibliographicCitation.issue26
local.bibliographicCitation.lastpage10140
local.bibliographicCitation.startpage10130
local.contributor.affiliationHutt, Oliver, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationMander, Lewis, College of Physical and Mathematical Sciences, ANU
local.contributor.authoremailu7500768@anu.edu.au
local.contributor.authoruidHutt, Oliver, u4017570
local.contributor.authoruidMander, Lewis, u7500768
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationu4005981xPUB181
local.identifier.citationvolume72
local.identifier.doi10.1021/jo701995u
local.identifier.scopusID2-s2.0-37549039870
local.identifier.uidSubmittedByu4005981
local.type.statusPublished Version

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