Highly efficient asymmetric bioreduction of 1-aryl-2-(azaaryl)ethanones. Chemoenzymatic synthesis of lanicemine

dc.contributor.author	Liz Guiral, Ramón
dc.contributor.author	Liardo, Elisa
dc.contributor.author	Rebolledo Vicente, Francisca
dc.date.accessioned	2020-01-23T08:17:41Z
dc.date.available	2020-01-23T08:17:41Z
dc.date.issued	2019
dc.identifier.citation	Organic and Biomolecular Chemistry, 17(35), p. 8214-8220 (2019); doi:10.1039/c9ob01616c
dc.identifier.issn	1477-0520
dc.identifier.uri	http://hdl.handle.net/10651/53805
dc.description.sponsorship	This work was supported by the Principado de Asturias (FC-GRUPIN-IDI2018000181). We also thank Dr Isabel Merino (NMR Unit of the Scientific and Technological Resources of the University of Oviedo) for advising and technical assistance on selective-1D TOCSY experiments.
dc.format.extent	p. 8214-8220
dc.language.iso	eng
dc.relation.ispartof	Organic and Biomolecular Chemistry, 17
dc.rights	© 2019 Royal Society of Chemistry
dc.rights	CC Reconocimiento - No Comercial - Sin Obra Derivada 4.0 Internacional
dc.rights.uri	http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.source	Scopus
dc.source.uri	https://www.scopus.com/inward/record.uri?eid=2-s2.0-85072037334&doi=10.1039%2fc9ob01616c&partnerID=40&md5=4288cecbe8c8a1bb7fa69adb96d11b50
dc.title	Highly efficient asymmetric bioreduction of 1-aryl-2-(azaaryl)ethanones. Chemoenzymatic synthesis of lanicemine
dc.type	journal article
dc.identifier.doi	10.1039/c9ob01616c
dc.relation.projectID	FC-GRUPIN-IDI2018000181
dc.relation.publisherversion	http://dx.doi.org/10.1039/c9ob01616c
dc.rights.accessRights	open access
dc.type.hasVersion	AM

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