Synthetic studies on amaryllidaceae and other terrestrially derived alkaloids

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dc.contributor.authorBanwell, Martin G.en
dc.contributor.authorGao, Nadia Yuqianen
dc.contributor.authorSchwartz, Brett D.en
dc.contributor.authorWhite, Lorenzo V.en
dc.date.accessioned2026-01-01T08:41:22Z
dc.date.available2026-01-01T08:41:22Z
dc.date.issued2012en
dc.description.abstractThe total syntheses of a wide range of terrestrially derived alkaloids, especially ones isolated from members of the Amaryllidaceae family, are described. Two recurring themes associated with these syntheses are the use of two types of building blocks, namely ring-fused cyclopropanes, especially geminally-dihalogenated ones, and enzymatically derived cis-1,2- dihydrocatechols. These have often served as precursors to 2-or 3-halogenated 2-cyclohexen-1-ols that are themselves engaged in cross-coupling reactions, radical addition-elimination processes and/or Claisen-or Overman-type rearrangements so as to construct the highly functionalized six-membered rings associated with the target alkaloids.en
dc.description.statusPeer-revieweden
dc.format.extent40en
dc.identifier.isbn9783642255281en
dc.identifier.issn0340-1022en
dc.identifier.otherPubMed:21972020en
dc.identifier.otherORCID:/0000-0003-2311-1080/work/161835315en
dc.identifier.scopus84856140930en
dc.identifier.urihttps://hdl.handle.net/1885/733799061
dc.language.isoenen
dc.relation.ispartofAlkaloid Synthesisen
dc.relation.ispartofseriesTopics in Current Chemistryen
dc.subjectγ-Lycoraneen
dc.subjectAlkaloidsen
dc.subjectAmabilineen
dc.subjectAmaryllidaceaeen
dc.subjectAspidospermidineen
dc.subjectBrunsvigineen
dc.subjectColchicineen
dc.subjectCorey-Winter reactionen
dc.subjectCross-couplingen
dc.subjectCyclopropaneen
dc.subjectepi-Maritinamineen
dc.subjectErythramineen
dc.subjectEschenmoser-Claisen rearrangementen
dc.subjectGalanthamineen
dc.subjectGrandirubrineen
dc.subjectHaemultineen
dc.subjectImerubrineen
dc.subjectIreland-Claisen rearrangementen
dc.subjectLycoricidineen
dc.subjectMaritinamineen
dc.subjectMitsunobu reactionen
dc.subjectNangustineen
dc.subjectNarciclasineen
dc.subjectOverman rearrangementen
dc.subjectPancracineen
dc.subjectPictet-Spengler reactionen
dc.subjectRadical cyclisationen
dc.subjectRhazinalen
dc.subjectRhazinilamen
dc.subjectSuzuki-Miyaura reactionen
dc.subjectUllmann reactionen
dc.subjectWittig reactionen
dc.titleSynthetic studies on amaryllidaceae and other terrestrially derived alkaloidsen
dc.typeBook chapteren
dspace.entity.typePublicationen
local.bibliographicCitation.lastpage202en
local.bibliographicCitation.startpage163en
local.contributor.affiliationBanwell, Martin G.; Wearable and Portable Devices, Research School of Chemistry, ANU College of Science and Medicine, The Australian National Universityen
local.contributor.affiliationGao, Nadia Yuqian; Wearable and Portable Devices, Research School of Chemistry, ANU College of Science and Medicine, The Australian National Universityen
local.contributor.affiliationSchwartz, Brett D.; Wearable and Portable Devices, Research School of Chemistry, ANU College of Science and Medicine, The Australian National Universityen
local.contributor.affiliationWhite, Lorenzo V.; Wearable and Portable Devices, Research School of Chemistry, ANU College of Science and Medicine, The Australian National Universityen
local.identifier.ariespublicationu4005981xPUB545en
local.identifier.doi10.1007/128_2011_217en
local.identifier.purefdd64b94-01dd-429b-9f6c-415ef4339e77en
local.identifier.urlhttps://www.scopus.com/pages/publications/84856140930en
local.type.statusPublisheden

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