[HTML][HTML] Unravelling a bench-stable zinc-amide compound as highly active multitasking catalyst for radical-mediated selective alk (en) ylation of unactivated …
The direct functionalization of unactivated organic moieties via C–C bond formation has long
fascinated synthetic chemists. Although base-metal systems are steadily emerging in this …
fascinated synthetic chemists. Although base-metal systems are steadily emerging in this …
A novel nanomagnetic palladium (II) complex of bisimidazolium-based Nheterocyclic carbene; An efficient heterogeneous catalyst for A3 coupling reactions
Herein, a novel nanomagnetic NHC-Palladium complex was successfully prepared applying
post-synthetic modification (PSM) condensation between Fe 3 O 4-support imidazole and a …
post-synthetic modification (PSM) condensation between Fe 3 O 4-support imidazole and a …
Synthesis and characterization of Markó-type (NHC) Pt (dvtms) complexes and their evaluation in the hydrosilylation reaction of alkenes
MJ Sauer, LF Richter, J Offorjindu, RM Reich… - Journal of …, 2024 - Elsevier
A series of Markó-type complexes of the structure (NHC) Pt (dvtms) were prepared (dvtms=
1, 1, 3, 3-tetramethyl-1, 3-divinyldisiloxane, NHC= N-heterocyclic carbene, Im= imidazole …
1, 1, 3, 3-tetramethyl-1, 3-divinyldisiloxane, NHC= N-heterocyclic carbene, Im= imidazole …
Synthesis of quinazolinone scaffolds via a zinc (ii)-stabilized amidyl radical-promoted deaminative approach
Herein, we report a solely ligand centered redox controlled protocol, utilizing a bench stable
zinc compound, for the efficient coupling of o-amino amides/esters with nitriles to afford …
zinc compound, for the efficient coupling of o-amino amides/esters with nitriles to afford …