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dc.contributor.authorGonzález, Antonio G.en_US
dc.contributor.authorCortés, Manuelen_US
dc.contributor.authorSuárez, Ernestoen_US
dc.date.accessioned2009-07-22T07:46:51Z-
dc.date.available2009-07-22T07:46:51Z-
dc.date.issued1974en_US
dc.identifier.citationChemical Communications 1974(11): 425b-426 (1974)en_US
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/10261/15184-
dc.description2 pages, 1 scheme.-
dc.description.abstractAcid treatment of trevoagenin A (1; 20R,24R) or B (1; 20S,24R) in aqueous alcohol gives a mixture of the lactone (2a) and its Z isomer.-
dc.description.sponsorshipThis work was performed within the Programme of Chemistry 1971 of the "Juan March" Foundation.-
dc.format.extent2373 bytes-
dc.format.extent134686 bytes-
dc.format.mimetypetext/plain-
dc.format.mimetypeapplication/pdf-
dc.language.isoengen_US
dc.publisherRoyal Society of Chemistry (UK)-
dc.rightsclosedAccessen_US
dc.titleAcid-catalysed rearrangements of trevoagenin A and Ben_US
dc.typeartículoen_US
dc.identifier.doi10.1039/C3974000425b-
dc.relation.publisherversionhttp://dx.doi.org/10.1039/C3974000425b-
dc.contributor.funderFundación Juan March-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100009154es_ES
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