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dc.contributor.authorPinedo Rivilla, Cristina 
dc.contributor.authorAleu Casatejada, Josefina 
dc.contributor.authorGonzález Collado, Isidro 
dc.contributor.otherQuímica Orgánicaen_US
dc.date.accessioned2015-05-18T11:29:03Z
dc.date.available2015-05-18T11:29:03Z
dc.date.issued2011-10-18T00:00:00Z
dc.identifier.issn0957-4166
dc.identifier.otherdoi:10.1016/j.tetasy.2011.09.010
dc.identifier.urihttp://hdl.handle.net/10498/17361
dc.description.abstractThe transformation of (E)-2-benzylideneindan-1-one 1 by the filamentous fungi Botrytis cinerea, Trichoderma viride, and Eutypa lata as biocatalysts was studied. The results showed the catalytic potential of these fungi in affording several hydroxylation and reduction products, three of them reported here for the first time. The absolute configuration of enantiomerically pure 2-benzylindane derivatives was determined.en_US
dc.formatapplication/pdf
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceTetrahedron: Asymmetry, 2011, vol. 22, pp. 1653–1657en_US
dc.subjectAsymmetric microbial conversionen_US
dc.subjectbenzylideneindan-1-oneen_US
dc.titleAsymmetric microbial conversion of (E)-2-benzylideneindan-1-one by the filamentous fungi Botrytis cinerea, Trichoderma viride, and Eutypa lataen_US
dc.typejournal articleen_US
dc.rights.accessRightsopen access
dc.identifier.doi10.1016/j.tetasy.2011.09.010


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