The Exploitation of Enzymatically-Derived cis-1,2-Dihydrocatechols and Related Compounds in the Synthesis of Biologically Active Natural Products

dc.contributor.authorTaher, Ehab
dc.contributor.authorBanwell, Martin
dc.contributor.authorBuckler, Joshua
dc.contributor.authorYan, Qiao
dc.contributor.authorLan, Ping
dc.date.accessioned2021-01-07T02:26:45Z
dc.date.issued2018
dc.date.updated2020-11-23T11:57:05Z
dc.description.abstractThe title compounds of the general form 1 can be produced at large scale and in essentially enantiomerically pure form (when X≠H) through the whole cell biotransformation of the corresponding aromatic. The “dense” and varied functionality associated with these metabolites mean that they have become increasingly useful chirons for the total synthesis of a range of natural product types. This personal account details the outcomes of a nearly three‐decade long campaign within our group to exploit these compounds in the synthesis of a diverse range of small molecule natural product targets. The work is subdivided according to the key transformation(s) employed in each synthesis. The development of newer chirons that “complement” the utility of the cis‐1,2‐dihydrocatechols are also described.en_AU
dc.description.sponsorshipWe thank the Australian Research Council, the Institute of Advanced Studies at the Australian National University, the Islamic Development Bank, the China Scholarship Council and Circa Pty Ltd (Melbourne) for generous financial support. The invaluable contributions of our colleagues who co-authored the articles listed below are also gratefully acknowledged.en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn1528-0691en_AU
dc.identifier.urihttp://hdl.handle.net/1885/219215
dc.language.isoen_AUen_AU
dc.publisherWileyen_AU
dc.relationhttp://purl.org/au-research/grants/arc/DP150101947en_AU
dc.rights© 2018 The Chemical Society of Japan & Wiley-VCH Verlag GmbH & Co. KGaA, Weinheimen_AU
dc.sourceThe Chemical Recorden_AU
dc.subjectChironsen_AU
dc.subjectCross-couplingsen_AU
dc.subjectDiels-Alder Reactionsen_AU
dc.subjectcis-1,2-Dihydrocatecholsen_AU
dc.subjectElectrophilic Additionsen_AU
dc.subjectEschenmoser-Claisen rearrangementsen_AU
dc.subjectNatural Productsen_AU
dc.subjectOxidative Cleavageen_AU
dc.titleThe Exploitation of Enzymatically-Derived cis-1,2-Dihydrocatechols and Related Compounds in the Synthesis of Biologically Active Natural Productsen_AU
dc.typeJournal articleen_AU
local.bibliographicCitation.issue2en_AU
local.bibliographicCitation.lastpage264en_AU
local.bibliographicCitation.startpage239en_AU
local.contributor.affiliationTaher, Ehab, College of Science, ANUen_AU
local.contributor.affiliationBanwell, Martin, College of Science, ANUen_AU
local.contributor.affiliationBuckler, Joshua, College of Science, ANUen_AU
local.contributor.affiliationYan, Qiao, College of Science, ANUen_AU
local.contributor.affiliationLan, Ping, Jinan Universityen_AU
local.contributor.authoremailmartin.banwell@anu.edu.auen_AU
local.contributor.authoruidTaher, Ehab, u5134756en_AU
local.contributor.authoruidBanwell, Martin, u9500594en_AU
local.contributor.authoruidBuckler, Joshua, u5064427en_AU
local.contributor.authoruidYan, Qiao, u5154190en_AU
local.description.embargo2037-12-31
local.description.notesImported from ARIESen_AU
local.identifier.absfor030503 - Organic Chemical Synthesisen_AU
local.identifier.absseo970103 - Expanding Knowledge in the Chemical Sciencesen_AU
local.identifier.ariespublicationa383154xPUB9194en_AU
local.identifier.citationvolume18en_AU
local.identifier.doi10.1002/tcr.201700064en_AU
local.identifier.scopusID2-s2.0-85037623631
local.identifier.uidSubmittedBya383154en_AU
local.publisher.urlhttps://www.wiley.com/en-gben_AU
local.type.statusPublished Versionen_AU

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