Olefin metathesis reactions with fluorinated substrates, catalysts, and solvents
S Fustero, A Simon-Fuentes, P Barrio… - Chemical …, 2015 - ACS Publications
Organofluorine compounds 1 have found increasing applications in key industrial fields
such as the pharmaceutical 2 and medicinal chemistry 3 or crop 4 and material sciences, 5 …
such as the pharmaceutical 2 and medicinal chemistry 3 or crop 4 and material sciences, 5 …
Recent advances in the application of ring-closing metathesis for the synthesis of unsaturated nitrogen heterocycles
EJ Groso, CS Schindler - Synthesis, 2019 - thieme-connect.com
This short review summarizes recent advances relating to the application of ring-closing
olefin-olefin and carbonyl-olefin metathesis reactions towards the synthesis of unsaturated …
olefin-olefin and carbonyl-olefin metathesis reactions towards the synthesis of unsaturated …
Photoinduced olefin diamination with alkylamines
S Govaerts, L Angelini, C Hampton… - Angewandte Chemie …, 2020 - Wiley Online Library
Vicinal diamines are ubiquitous materials in organic and medicinal chemistry. The direct
coupling of olefins and amines would be an ideal approach to construct these motifs …
coupling of olefins and amines would be an ideal approach to construct these motifs …
Ligand-controlled regioselectivity in the hydrothiolation of alkynes by rhodium N-heterocyclic carbene catalysts
A Di Giuseppe, R Castarlenas… - Journal of the …, 2012 - ACS Publications
Rh–N-heterocyclic carbene compounds [Rh (μ-Cl)(IPr)(η2-olefin)] 2 and RhCl (IPr)(py)(η2-
olefin)(IPr= 1, 3-bis (2, 6-diisopropylphenyl) imidazol-2-carbene, py= pyridine, olefin …
olefin)(IPr= 1, 3-bis (2, 6-diisopropylphenyl) imidazol-2-carbene, py= pyridine, olefin …
Cationic ruthenium (II)-CNC pincer complexes as phosphine-free catalysts for nitrile hydration to amides in aqueous medium
We report the synthesis, characterization, and catalytic activity of a series of electron-rich,
phosphine-free complexes featuring multiple N-heterocyclic carbene (NHC) ligands, namely …
phosphine-free complexes featuring multiple N-heterocyclic carbene (NHC) ligands, namely …
The activation mechanism of Ru–Indenylidene complexes in olefin metathesis
CA Urbina-Blanco, A Poater, T Lebl… - Journal of the …, 2013 - ACS Publications
Olefin metathesis is a powerful tool for the formation of carbon–carbon double bonds.
Several families of well-defined ruthenium (Ru) catalysts have been developed during the …
Several families of well-defined ruthenium (Ru) catalysts have been developed during the …
Synthesis and study of olefin metathesis catalysts supported by redox-switchable diaminocarbene [3] ferrocenophanes
CD Varnado, EL Rosen, MS Collins, VM Lynch… - Dalton …, 2013 - pubs.rsc.org
A redox-switchable ligand, N, N′-dimethyldiaminocarbene [3] ferrocenophane (5), was
synthesized and incorporated into a series of Ir-and Ru-based complexes. Electrochemical …
synthesized and incorporated into a series of Ir-and Ru-based complexes. Electrochemical …
Comparison of different ruthenium–alkylidene bonds in the activation step with N-heterocyclic carbene Ru-catalysts for olefins metathesis
Density functional theory calculations have been used to investigate the activation steps
involving three of the most used alkylidene groups in Ru-catalysts for olefins metathesis …
involving three of the most used alkylidene groups in Ru-catalysts for olefins metathesis …
How does the addition of steric hindrance to a typical N-heterocyclic carbene ligand affect catalytic activity in olefin metathesis?
Density functional theory (DFT) calculations were used to predict and rationalize the effect of
the modification of the structure of the prototype 1, 3-bis (2, 6-diisopropylphenyl) imidazol-2 …
the modification of the structure of the prototype 1, 3-bis (2, 6-diisopropylphenyl) imidazol-2 …
Low Catalyst Loading in Ring‐Closing Metathesis Reactions
R Kadyrov - Chemistry–A European Journal, 2013 - Wiley Online Library
An efficient procedure is described for ring‐closing metathesis reactions. A conversion of
95% for diethyl diallylmalonate in dilute solution could be achieved within a few minutes …
95% for diethyl diallylmalonate in dilute solution could be achieved within a few minutes …