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Six-Membered Ring Systems: With O and/or S Atoms

dc.contributor.authorSantos, Clementina M.M.
dc.contributor.authorSilva, Artur
dc.date.accessioned2017-11-09T15:57:08Z
dc.date.available2017-11-09T15:57:08Z
dc.date.issued2017
dc.description.abstractIn 2016, the large variety of publications focused on the synthesis of O- and S-6-membered ring systems highlights the importance and popularity of these heterocyclic compounds. Reviews on natural products covered the origins and medicinal use of avermectins (16AGE10190), discovery, isolation, characterization and application of artemisinin (16AGE10210), biosynthesis of fungal meroterpenoids (16NPR26), isolation, biological properties, and synthesis of dimeric pyranonaphthoquinones (16EJO5778), and peroxide and peroxide-derived polyketide metabolites from marine sponges (16NPR861). Late-stage convergent annulation reactions (16T3345) and rhodium-catalyzed annulation reactions of arenes with alkynes via weak chelation-assisted CdH activation (16CC2872) for the synthesis of several natural six-membered oxacycles have also been reviewed. New approaches for the synthesis of naturally occurring bioactive pyran derivatives have appeared. Different routes have been established for the total synthesis of tetrahydropyran-containing natural compounds brevisamide (16EJO2300, 16JOC3799), (±)-centrolobine (16SL2221), (−)-clavosolide A (16AGE2498), (+)-decarestrictine L (16TL4368), decytospolide A, B, and their C-3 epimers (16S765), goniodomin A (16JOC2213), herboxidiene (16OBC6212), irciniastatins (16JOC1930), (−)-lasonolide A (16JA11690), (−)-luminacin D (16JOC3818), (−)-mandelalide A (16JA770, 16JA3675), isomandelalide A (16JA770), thailanstatin A (16JA7532); of the 2H-pyran- 2-ones sibirinone, (E)-6-(pent-1-en-1-yl)-2H-pyran-2-one and (E)-6- (hept-1-en-1-yl)-2H-pyran-2-one (16JOC10357); of the 5,6-dihydropyran- 2-one derivatives cryptomoscatone F1 (16S1561), cryptorigidifoliol B (16TL2100), cryptorigidifoliol E (16S4213), 8-methoxygoniodiol (16S4300), pectinolides A, C, and H (16HCA247); and of the tetrahydropyran-2-one derivatives (−)-(S)-goniothalamin and (−)-leiocarpin (16SC187), helicascolides A, B, and C (16AGE5765), isodaphlongamine H (16AGE2577), and (−)-malyngolide and its C-5 epimer (16HCA267).pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationSantos, Clementina M.M.; Silva, Artur (2017). Six-membered ring systems: with O and/or S atoms. In Progress in Heterocyclic Chemistry. Amsterdam: Elsevier, Vol. 29, Chapter 6.4, p. 519-578. ISBN 978-0-08-102310-5pt_PT
dc.identifier.doi10.1016/B978-0-08-102310-5.00015-1pt_PT
dc.identifier.isbn978-0-08-102310-5
dc.identifier.isbn978-0-08-102311-2
dc.identifier.urihttp://hdl.handle.net/10198/14614
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherElsevierpt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.titleSix-Membered Ring Systems: With O and/or S Atomspt_PT
dc.typebook part
dspace.entity.typePublication
oaire.citation.conferencePlaceSharjah, UAEpt_PT
oaire.citation.endPage578pt_PT
oaire.citation.startPage519pt_PT
oaire.citation.titleProgress in Heterocyclic Chemistrypt_PT
oaire.citation.volume29pt_PT
person.familyNameSantos
person.givenNameClementina M.M.
person.identifier.ciencia-id9018-DB9C-C590
person.identifier.orcid0000-0003-4380-7990
person.identifier.scopus-author-id7201458663
rcaap.rightsopenAccesspt_PT
rcaap.typebookPartpt_PT
relation.isAuthorOfPublication64f662b6-775d-4ea0-bfd7-f527af0ac1a0
relation.isAuthorOfPublication.latestForDiscovery64f662b6-775d-4ea0-bfd7-f527af0ac1a0

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