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dc.contributor.authorZou, Yupiao
dc.contributor.authorHan, Jianlin ORCID
dc.contributor.authorSaghyan, Ashot S.
dc.contributor.authorMkrtchyan, Anna F.
dc.contributor.authorKonno, Hiroyuki
dc.contributor.authorMoriwaki, Hiroki
dc.contributor.authorIzawa, Kunisuke
dc.contributor.authorSoloshonok, Vadym Anatolievch ORCID
dc.date.accessioned2020-07-13T10:27:54Z
dc.date.available2020-07-13T10:27:54Z
dc.date.issued2020-06-12
dc.identifier.citationMolecules 25(12) : (2020) // Article ID 2739es_ES
dc.identifier.issn1420-3049
dc.identifier.urihttp://hdl.handle.net/10810/45443
dc.description.abstractTailor-made amino acids are indispensable structural components of modern medicinal chemistry and drug design. Consequently, stereo-controlled preparation of amino acids is the area of high research activity. Over last decade, application of Ni(II) complexes of Schiff bases derived from glycine and chiral tridentate ligands has emerged as a leading methodology for the synthesis of various structural types of amino acids. This review article summarizes examples of asymmetric synthesis of tailor-made α-amino acids via the corresponding Ni(II) complexes, reported in the literature over the last four years. A general overview of this methodology is provided, with the emphasis given to practicality, scalability, cost-structure and recyclability of the chiral tridentate ligands.es_ES
dc.description.sponsorshipThis research was funded by the National Natural Science Foundation of China (No. 21761132021), and IKERBASQUE, Basque Foundation for Science.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/
dc.subjecttailor-made amino acidses_ES
dc.subjectSchiff baseses_ES
dc.subjectasymmetric synthesises_ES
dc.subjectchiral tridentate ligandses_ES
dc.subjectsquare-planar Ni(II) complexeses_ES
dc.titleAsymmetric Synthesis of Tailor-Made Amino Acids Using Chiral Ni(II) Complexes of Schiff Bases. An Update of the Recent Literaturees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2020-06-30T16:29:20Z
dc.rights.holder2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/1420-3049/25/12/2739/htmes_ES
dc.identifier.doi10.3390/molecules25122739
dc.departamentoesQuímica orgánica I
dc.departamentoeuKimika organikoa I


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2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).