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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.accessioned2015-03-02T10:18:30Z
dc.date.available2015-03-02T10:18:30Z
dc.date.issued2014
dc.description.abstractThe large number of publications in 2013 dedicated to O- and S-six-membered ring systems highlights the importance of these heterocycles. The chemistry and biological activity of the family of plants Hyacinthaceae, and of their homoisoflavanone main constituents (13NPR1165) and of the fungal polyketide metabolites azaphilones (13CR4755) and various aspects on the isolation, synthesis, and biological activity of angular tricyclic benzofurans and related natural products of fungal origin (13NPR941) and marine polyketide psymberin (13AGE10960) have been surveyed. A review on the history of natural product synthesis covers the early phase of this subject, where it was the method of choice to confirm the proposed structure of a natural product, to the challenges of the twenty-first century (13AGE123).por
dc.identifier.citationSantos, Clementina M.M.; Silva, Artur M. S. (2014). Six-membered ring systems: with O and/or S atoms. In Progress in Heterocyclic Chemistry. Vol 26. Chapter 6.4. [S.l.]: Elsevier, p. 463-520. ISBN 978-0-08-100017-5por
dc.identifier.doi10.1016/B978-0-08-100017-5.00015-7
dc.identifier.isbn978-0-08-100017-5
dc.identifier.urihttp://hdl.handle.net/10198/11713
dc.language.isoporpor
dc.peerreviewedyespor
dc.publisherElsevierpor
dc.subjectOxygen 6-membered heterocyclespor
dc.subjectSulfur 6-membered heterocyclespor
dc.titleSix-membered ring systems: with O and/or S atomspor
dc.typebook part
dspace.entity.typePublication
oaire.citation.endPage520por
oaire.citation.startPage463por
oaire.citation.titleProgress in Heterocyclic Chemistrypor
oaire.citation.volume26por
person.familyNameSantos
person.givenNameClementina
person.identifier.ciencia-id9018-DB9C-C590
person.identifier.orcid0000-0003-4380-7990
person.identifier.scopus-author-id7201458663
rcaap.rightsopenAccesspor
rcaap.typebookPartpor
relation.isAuthorOfPublication64f662b6-775d-4ea0-bfd7-f527af0ac1a0
relation.isAuthorOfPublication.latestForDiscovery64f662b6-775d-4ea0-bfd7-f527af0ac1a0

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