Results 171 to 180 of about 14,653 (264)

Tricyanoborane-Functionalized Anionic N-Heterocyclic Carbenes: Adjustment of Charge and Stereo-Electronic Properties. [PDF]

Chemistry, 2022
Zapf L, Peters S, Bertermann R, Radius U, Finze M.   +4 more
europepmc   +1 more source

Surface Characterization of N-Heterocyclic Carbenes on Gold and Silver: Exploring Distinct Crystalline Facets. [PDF]

Chemphyschem
Mahapatra S, Li L, Jiang N.
europepmc   +1 more source

Free N-heterocyclic carbenes from Brønsted acidic ionic liquids: Direct detection by electrospray ionization mass spectrometry. [PDF]

Rapid Commun Mass Spectrom, 2022
Salvitti C, Pepi F, Managò M, Bortolami M, Michenzi C, Chiarotto I, Troiani A, de Petris G.   +7 more
europepmc   +1 more source

Catalytically Active Gold Nanomaterials Stabilized by N-heterocyclic Carbenes. [PDF]

Chem Asian J, 2021
Eisen C, Chin JM, Reithofer MR.
europepmc   +1 more source

IPr*^diNHC: Sterically Adaptable Dinuclear N-Heterocyclic Carbenes. [PDF]

Inorg Chem
Halikowska-Tarasek K, Ochędzan-Siodłak W, Dziuk B, Szostak R, Szostak M, Bisz E.   +5 more
europepmc   +1 more source

Halogen Complexes of Anionic N-Heterocyclic Carbenes. [PDF]

Chemistry, 2021
Frosch J, Koneczny M, Bannenberg T, Tamm M.   +3 more
europepmc   +1 more source

Bridged Pyrroloindole‐CAYC‐Gold Complexes: Harnessing Weak Secondary Intramolecular Au···H−C(sp3) Interactions in Gold(I) Catalysis

Angewandte Chemie, Volume 138, Issue 17, 20 April 2026.
We present a new class of electronically and sterically hindered N‐heterocyclic carbenes, referred to as bridged cyclic (amino)ylide carbene (bCAYC), where 9H‐pyrrolo[1,2‐a]indole acted as carbene core and diaryl sulfonium as ylide partner. Corresponding bCAYC‐Au(I) exhibits a weak secondary intramolecular Au···H−C(sp3) interaction as a secondary ...
Sourav Sekhar Bera, Anurag Kumar, Pengcheng Gao, Sanghamitra Das, Roger Lalancette, Roman Szostak, Michal Szostak   +6 more
wiley   +2 more sources

N-heterocyclic carbenes as clickable molecular anchors for electrochemical surface functionalization of metals and glassy carbon. [PDF]

Chem Sci
Juneau A, Nezamzadeh A, Laberge B, Messina A, Lomax J, Suduwella TM, Kaur J, Singh V, Aloisio MD, Ragogna PJ, Crudden CM, Mauzeroll J.   +11 more
europepmc   +1 more source

Formation of Breslow Intermediates from N-Heterocyclic Carbenes and Aldehydes Involves Autocatalysis by the Breslow Intermediate, and a Hemiacetal. [PDF]

Angew Chem Int Ed Engl, 2022
Wessels A, Klussmann M, Breugst M, Schlörer NE, Berkessel A.   +4 more
europepmc   +1 more source

Pd‐Catalyzed C─C Bond Borylation of Biphenylenes Leading to Tri‐Ortho‐Substituted Biaryls

Chemistry – A European Journal, Volume 32, Issue 16, 25 April 2026.
Palladium‐catalyzed ring‐opening C─C borylation of 1‐substituted biphenylenes yields a range of o,o,o′‐trisubstituted biaryls with two ortho‐boryl groups via selective cleavage of the least hindered C─C bond. The resulting diborylated products are readily amenable to sequential, site‐selective postfunctionalization.
Robyn V. Presland, Konstantin V. Luzyanin, Luke A. Wilkinson, Oliver L. Jacobs, Nathan R. Halcovitch, Alexey G. Sergeev   +5 more
wiley   +1 more source