dc.creatorde la Sovera, Victoria
dc.creatorSuescun, Leopoldo
dc.creatorBellomo Peraza, Ana Ines
dc.creatorGonzález, David
dc.date.accessioned2018-07-04T15:28:05Z
dc.date.accessioned2018-11-06T11:18:54Z
dc.date.available2018-07-04T15:28:05Z
dc.date.available2018-11-06T11:18:54Z
dc.date.created2018-07-04T15:28:05Z
dc.date.issued2017-07-17
dc.identifierde la Sovera, Victoria; Suescun, Leopoldo; Bellomo Peraza, Ana Ines; González, David; Chemoenzymatic Synthesis of Triazololactams Structurally Related to Pancratistatin; Wiley VCH Verlag; European Journal of Organic Chemistry; 2017; 27; 17-7-2017; 3912-3916
dc.identifier1434-193X
dc.identifierhttp://hdl.handle.net/11336/51172
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1848302
dc.description.abstractFour tricyclic lactams that structurally resemble alkaloids with the pancratistatin skeleton were synthetized from bromobenzene by a chemoenzymatic strategy. The sequence involved enzymatic dihydroxylation, efficient stereodirected oxidation of double bonds, inter- or intramolecular Huisgen cycloaddition, and a solvent-free cyclization. The complex structures were obtained in high chemical and optical purity and may be good candidates for biological testing.
dc.languageeng
dc.publisherWiley VCH Verlag
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1002/ejoc.201700334
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/ejoc.201700334
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectALKALOIDS
dc.subjectASYMMETRIC SYNTHESIS
dc.subjectCHEMOENZYMATIC SYNTHESIS
dc.subjectCLICK CHEMISTRY
dc.subjectCYCLOADDITION
dc.titleChemoenzymatic Synthesis of Triazololactams Structurally Related to Pancratistatin
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


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