Chemoselective Heterogeneous Hydrogenation of Sulfur Containing Quinolines under Mild Conditions.

Lückemeier L; De Vos T; Schlichter L; Gutheil C; Daniliuc CG; Glorius F

Forschungsartikel (Zeitschrift) | Peer reviewed

Zusammenfassung

Sulfur, alongside oxygen and nitrogen, holds a prominent position as one of the key heteroatoms in nature and medicinal chemistry. Its significance stems from its ability to adopt different oxidation states, rendering it valuable as both a polarity handle and a hydrogen bond donor/acceptor. Nevertheless, the poisonous nature of its free electron pairs makes sulfur containing substrates inaccessible for many catalytic protocols. Strong and (at low temperatures) irreversible chemisorption to the catalyst's surface is in particular detrimental for heterogeneous catalysts, possessing only few catalytically active sites. Herein, we present a novel heterogeneous Ru-S catalyst that tolerates multiple sulfur functionalities, including thioethers, thiophenes, sulfoxides, sulfones, sulfonamides, and sulfoximines, in the hydrogenation of quinolines. The utility of the products was further demonstrated by subsequent diversifications of the sulfur functionalities.

Details zur Publikation

FachzeitschriftJournal of the American Chemical Society (J. Am. Chem. Soc.)
Jahrgang / Bandnr. / Volume146
Ausgabe / Heftnr. / Issue9
Seitenbereich5864-5871
StatusVeröffentlicht
Veröffentlichungsjahr2024 (06.03.2024)
Sprache, in der die Publikation verfasst istEnglisch
DOI10.1021/jacs.3c11163
Link zum Volltexthttps://pubs.acs.org/doi/10.1021/jacs.3c11163
StichwörterAnions; Catalysts; Hydrogenation; Quinolines; Sulfur

Autor*innen der Universität Münster

Daniliuc, Constantin-Gabriel
Organisch-Chemisches Institut
Glorius, Frank
Professur für Organische Chemie (Prof. Glorius)
Gutheil, Christian
Professur für Organische Chemie (Prof. Glorius)
Lückemeier, Lukas
Professur für Organische Chemie (Prof. Glorius)
Schlichter, Lisa
Organisch-Chemisches Institut