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A total synthesis of the marine alkaloid ningalin B from ( S )-proline

Hasse, Katrin; Willis, Anthony; Banwell, Martin

Description

The title alkaloid 1 has been synthesized from (S)-proline (2) using a sequence of reactions involving oxidative bromination (of 2), N-alkylation, SuzukiMiyaura cross-coupling, and bromination steps.

dc.contributor.authorHasse, Katrin
dc.contributor.authorWillis, Anthony
dc.contributor.authorBanwell, Martin
dc.date.accessioned2015-12-10T22:30:43Z
dc.identifier.issn0004-9425
dc.identifier.urihttp://hdl.handle.net/1885/55216
dc.description.abstractThe title alkaloid 1 has been synthesized from (S)-proline (2) using a sequence of reactions involving oxidative bromination (of 2), N-alkylation, SuzukiMiyaura cross-coupling, and bromination steps.
dc.publisherCSIRO Publishing
dc.sourceAustralian Journal of Chemistry
dc.subjectKeywords: Marine alkaloids; N-alkylation; Oxidative bromination; Suzuki-Miyaura cross-coupling; Total synthesis; Hydrocarbons; Synthesis (chemical)
dc.titleA total synthesis of the marine alkaloid ningalin B from ( S )-proline
dc.typeJournal article
local.description.notesImported from ARIES
local.identifier.citationvolume62
dc.date.issued2009
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationu4005981xPUB322
local.type.statusPublished Version
local.contributor.affiliationHasse, Katrin, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationWillis, Anthony, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationBanwell, Martin, College of Physical and Mathematical Sciences, ANU
local.description.embargo2037-12-31
local.bibliographicCitation.issue7
local.bibliographicCitation.startpage683
local.bibliographicCitation.lastpage691
local.identifier.doi10.1071/CH09158
dc.date.updated2016-02-24T10:23:03Z
local.identifier.scopusID2-s2.0-67949118730
local.identifier.thomsonID000267887700011
CollectionsANU Research Publications

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