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Por favor, use este identificador para citar o enlazar este ítem: https://ri.ufs.br/jspui/handle/riufs/26095
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dc.contributor.authorJesus, Hugo César Ramos de-
dc.contributor.authorJeller, Alex Haroldo-
dc.contributor.authorDebonsi, Hosana Maria-
dc.contributor.authorAlves, Pericles Barreto-
dc.contributor.authorPorto, André Luiz Meleiro-
dc.date.accessioned2026-09-11T20:52:14Z-
dc.date.available2026-09-11T20:52:14Z-
dc.date.issued2017-
dc.identifier.citationJESUS, H. C. R. et al. Multiple monohydroxylation products from rac-camphor by marine fungus Botryosphaeria sp. isolated from marine alga bostrychia radicans. Journal of the Brazilian Chemical Society, São Paulo, v. 28, n. 3, p. 498–504, 2017. DOI: http://dx.doi.org/10.21577/0103-5053.20160262. Disponível em: https://www.scielo.br/j/jbchs/a/wvzCNnh6hfRw9JpgDcBbdYw/abstract/?lang=en. Acesso em: 11 set. 2026.pt_BR
dc.identifier.issn1678-4790-
dc.identifier.urihttps://ri.ufs.br/jspui/handle/riufs/26095-
dc.languageengpt_BR
dc.publisherSociedade Brasileira de Químicapt_BR
dc.relation.ispartofJournal of the Brazilian Chemical Societypt_BR
dc.subjectTerpeneeng
dc.subjectHydroxylationeng
dc.subjectBiocatalysiseng
dc.subjectMarine endophytic fungieng
dc.titleMultiple monohydroxylation products from rac-camphor by marine fungus Botryosphaeria sp. isolated from marine alga bostrychia radicanspt_BR
dc.typeArtigopt_BR
dc.identifier.licenseCreative Commons Atribuição 4.0 Internacional (CC BY 4.0)pt_BR
dc.description.resumoThis manuscript describes the biooxidation of rac-camphor using whole cells of marine-derived fungus Botryosphaeria sp. CBMAI 1197. The main biotransformation products of this monoterpene were achieved via a hydroxylation reaction and occurred with 5 days of rac-camphor incubation. Products were identified by means of gas chromatography mass spectrometry (GC-MS) and nuclear magnetic resonance (NMR) data. The major hydroxylated products were 6-endo-hydroxycamphor, 6-exo-hydroxycamphor, 5-exo-hydroxycamphor, 5-endo-hydroxycamphor, 3-exo-hydroxycamphor and 8-hydroxycamphor. The 6-exo-hydroxycamphor was obtained through a retro-aldol reaction when 6-endo-hydroxycamphor was maintained in presence of CDCl3; this isomerization was confirmed by 1 H NMR and GC-MS data.pt_BR
dc.description.localSão Paulopt_BR
dc.identifier.doihttps://doi.org/10.21577/0103-5053.20160262-
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