Total syntheses of spirocyclic PKS-NRPS-based fungal metabolites

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dc.contributor.authorJo, Deokheeko
dc.contributor.authorHan, Sunkyuko
dc.date.accessioned2018-07-24T03:00:10Z-
dc.date.available2018-07-24T03:00:10Z-
dc.date.created2018-06-20-
dc.date.created2018-06-20-
dc.date.created2018-06-20-
dc.date.issued2018-05-
dc.identifier.citationCHEMICAL COMMUNICATIONS, v.54, no.50, pp.6750 - 6758-
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/10203/244582-
dc.description.abstractSince the first isolation of pseurotin A in 1976, over twenty five spirocyclic PKS-NRPS-based (polyketide synthase-nonribosomal peptide synthetase-based) fungal natural products have been discovered to date. The common 1-oxa-7-azaspiro[4.4]non-2-ene-4,6-dione core of this family of natural products has served as a platform for the development of novel chemistry and resulted in the development of numerous new reactivities and synthetic strategies. Herein, we delineate all reported syntheses of spirocyclic PKS-NRPS-based fungal metabolites including our own recent contributions on this subject. We showcase how a biosynthetic consideration could lead to concise synthetic routes to this family of natural products.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleTotal syntheses of spirocyclic PKS-NRPS-based fungal metabolites-
dc.typeArticle-
dc.identifier.wosid000436029000021-
dc.identifier.scopusid2-s2.0-85048787949-
dc.type.rimsART-
dc.citation.volume54-
dc.citation.issue50-
dc.citation.beginningpage6750-
dc.citation.endingpage6758-
dc.citation.publicationnameCHEMICAL COMMUNICATIONS-
dc.identifier.doi10.1039/C8CC02315H-
dc.contributor.localauthorHan, Sunkyu-
dc.description.isOpenAccessN-
dc.type.journalArticleReview-
dc.subject.keywordPlusASYMMETRIC TOTAL-SYNTHESIS-
dc.subject.keywordPlusPSEUDEUROTIUM-OVALIS STOLK-
dc.subject.keywordPlusENANTIOSELECTIVE MICHAEL ADDITIONS-
dc.subject.keywordPlusPSEUROTIN-A-
dc.subject.keywordPlusABSOLUTE-CONFIGURATION-
dc.subject.keywordPlusASPERGILLUS-FUMIGATUS-
dc.subject.keywordPlusSTEREOCONTROLLED SYNTHESIS-
dc.subject.keywordPlusBENZYLMAGNESIUM CHLORIDE-
dc.subject.keywordPlus1,3-DICARBONYL COMPOUNDS-
dc.subject.keywordPlusANGIOGENESIS INHIBITOR-
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