
ul. F. Joliot-Curie 14
roman.szostak@uwr.edu.pl
tel. +48 71 375 72 38, +48 71 375 72 04
Interested
- spectroscopy
- chemometrics
- organic chemistry
- amides
- general chemistry
- cross coupling
- amide bond
- n−c activation
- n–c activation
- n c o activation
Scientific discipline
- chemical sciences
Latest publications
- Acyl fluorides as direct precursors to fluoride ketyl radicals: reductive deuteration using SmI2 and D2O.
- 17O NMR and 15N NMR chemical shifts of sterically-hindered amides: ground-state destabilization in amide electrophilicity.
- CAAC–IPr*: easily accessible, highly sterically-hindered cyclic (alkyl)(amino)carbenes
- IPr# – highly hindered, broadly applicable N-heterocyclic carbenes.
- L‐Shaped Heterobidentate Imidazo[1,5‐a]pyridin‐3‐ylidene (N,C)‐Ligands for Oxidant‐Free AuI/AuIII Catalysis
- ItOct (ItOctyl) – pushing the limits of ItBu: highly hindered electron-rich N-aliphatic N-heterocyclic carbenes
- Copper(I)–thiazol-2-ylidenes: highly reactive N-heterocyclic carbenes for the hydroboration of terminal and internal alkynes. Ligand development, synthetic utility, and mechanistic studies
- Structures of the Most Twisted Thioamide and Selenoamide: Effect of Higher Chalcogens of Twisted Amides on N−C(X) Resonance
- Wingtip‐Flexible N‐Heterocyclic Carbenes: Unsymmetrical Connection between IMes and IPr
- Palladium-NHC (NHC = N-heterocyclic Carbene)-Catalyzed Suzuki–Miyaura Cross-Coupling of Alkyl Amides.
- Ring-opening olefin metathesis of twisted amides: activation of amide bonds by C═C cleavage.
- N-acylcarbazoles and N-acylindoles: electronically activated amides for N–C(O) cross-coupling by Nlp to Ar conjugation switch.
- Preference of cis-thioamide structure in N-thioacyl-N-methylanilines.
- Quantitative Determination of Diosmin in Tablets by Infrared and Raman Spectroscopy
- Comparative profiling of serum biomarkers and ATR-FTIR spectroscopy for differential diagnosis of patients with rheumatoid and psoriatic arthritis − a pilot study
- [IPr#–PEPPSI]: A Well-Defined, Highly Hindered and Broadly Applicable Pd(II)–NHC (NHC = N-Heterocyclic Carbene) Precatalyst for Cross-Coupling Reactions
- Sterically hindered ketones via palladium-catalyzed Suzuki–Miyaura cross-coupling of amides by N–C(O) activation.
- IPr*Oxa – a new class of sterically-hindered, wingtip-flexible N,C-chelating oxazole-donor N-heterocyclic carbene ligands
- [Au(Np#)Cl]: highly reactive and broadly applicable Au(I)–NHC catalysts for alkyne π-activation reactions
- Chemistry of bridged lactams: recent developments.