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Highly chemoselective homologative assembly of the α-substi..:
Monika Malik (Department of Pharmaceutical Sciences, Faculty of Life Sciences, University of Vienna)
;
Raffaele Senatore (Department of Pharmaceutical Sciences, Faculty of Life Sciences, University of Vienna)
;
Davide Castiglione (Department of Chemistry, University of Turin)
..
hdl:11353/10.2036110. , 2023
Link:
https://doi.org/10.1039/D3CC03326K
RT Journal T1
Highly chemoselective homologative assembly of the α-substituted methylsulfinamide motif from N -sulfinylamines
UL https://suche.suub.uni-bremen.de/peid=base-ftunivwiendc:oai:phaidra.univie.ac.at:o:2036110&Exemplar=1&LAN=DE A1 Monika Malik (Department of Pharmaceutical Sciences, Faculty of Life Sciences, University of Vienna) A1 Raffaele Senatore (Department of Pharmaceutical Sciences, Faculty of Life Sciences, University of Vienna) A1 Davide Castiglione (Department of Chemistry, University of Turin) A1 Alexander Roller-Prado (Department of Inorganic Chemistry - functional materials, Faculty of Chemistry, University of Vienna) A1 Vittorio Pace (Department of Pharmaceutical Sciences, Faculty of Life Sciences, University of Vienna) PB Royal Society of Chemistry (RSC) YR 2023 K1 Materials Chemistry K1 Metals and Alloys K1 Surfaces K1 Coatings and Films K1 General Chemistry K1 Ceramics and Composites K1 Electronic K1 Optical and Magnetic Materials K1 Catalysis JF hdl:11353/10.2036110 LK http://dx.doi.org/https://doi.org/10.1039/D3CC03326K DO https://doi.org/10.1039/D3CC03326K SF ELIB - SuUB Bremen
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