Cinchona‐Based Hydrogen‐Bond Donor Organocatalyst Metal Complexes: Asymmetric Catalysis and Structure Determination

Nagy, Sándor [Nagy, Sándor (Szerves kémia), author] Department of Organic Chemistry and Technology (BUTE / FCTB); Richter, Dóra [Richter, Dóra (Szerves kémia), author] Department of Organic Chemistry and Technology (BUTE / FCTB); Dargó, Gyula [Dargó, Gyula (szerves kémia), author] Department of Organic Chemistry and Technology (BUTE / FCTB); Orbán, Balázs; Gémes, Gergő; Höltzl, Tibor [Höltzl, Tibor (Kémia, nanotechno...), author] Department of Inorganic and Analytical Chemistry (BUTE / FCTB); ELKH-BME Computation Driven Chemistry (BUTE / FCTB / DIAC); Garádi, Zsófia [Garádi, Zsófia (NMR spektroszkópia), author] Department of Pharmacognosy (SU / FP); Fehér, Zsuzsanna [Fehér, Zsuzsanna (szerves kémia), author] Department of Organic Chemistry and Technology (BUTE / FCTB); Kupai, József ✉ [Kupai, József (Szerves kémia), author] Department of Organic Chemistry and Technology (BUTE / FCTB)

English Article (Journal Article) Scientific
Published: CHEMISTRYOPEN 2191-1363 2191-1363 13 (4) Paper: e202300180 , 10 p. 2024
  • SJR Scopus - Chemistry (miscellaneous): Q2
Identifiers
Fundings:
  • (FK138037)
  • National Laboratory of Translational Neuroscience(RRF-2.3.1-21-2022-00015)
  • Nemzeti Gyógyszerkutatási és Fejlesztési Laboratórium(PharmaLab) Funder: NRDIO
Subjects:
  • Chemical sciences
In this study, we describe the synthesis of cinchona (thio)squaramide and a novel cinchona thiourea organocatalyst. These catalysts were employed in pharmaceutically relevant catalytic asymmetric reactions, such as Michael, Friedel–Crafts, and A 3 coupling reactions, in combination with Ag(I), Cu(II), and Ni(II) salts. We identified several organocatalyst‐metal salt combinations that led to a significant increase in both yield and enantioselectivity. To gain insight into the active catalyst species, we prepared organocatalyst‐metal complexes and characterized them using HRMS, NMR spectroscopy, and quantum chemical calculations (B3LYP‐D4/def2‐TZVP), which allowed us to establish a structure‐activity relationship.
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2025-04-26 01:27