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Carbon-13 NMR chemical shift: a descriptor for electronic structure and reactivity of organometallic compounds
Conspectus Metal-bonded carbon atoms in metal–alkyl, metal–carbene/alkylidene, and
metal–carbyne/alkylidyne species often show significantly more deshielded isotropic …
metal–carbyne/alkylidyne species often show significantly more deshielded isotropic …
Improved Ruthenium Catalysts for Z-Selective Olefin Metathesis
BK Keitz, K Endo, PR Patel, MB Herbert… - Journal of the …, 2012 - ACS Publications
Several new C–H-activated ruthenium catalysts for Z-selective olefin metathesis have been
synthesized. Both the carboxylate ligand and the aryl group of the N-heterocyclic carbene …
synthesized. Both the carboxylate ligand and the aryl group of the N-heterocyclic carbene …
Recent advancement on the mechanism of olefin metathesis by Grubbs catalysts: A computational perspective
The second-generation Grubbs catalyst contains N-heterocyclic carbene (NHC) coordinated
to Ru center. Various such complexes have been employed as catalysts for the olefin …
to Ru center. Various such complexes have been employed as catalysts for the olefin …
Key processes in ruthenium-catalysed olefin metathesis
DJ Nelson, S Manzini, CA Urbina-Blanco… - Chemical …, 2014 - pubs.rsc.org
While the fundamental series of [2+ 2] cycloadditions and retro [2+ 2] cycloadditions that
make up the pathways of ruthenium-catalysed metathesis reactions is well-established, the …
make up the pathways of ruthenium-catalysed metathesis reactions is well-established, the …
On the mechanism of the initiation reaction in Grubbs–Hoveyda complexes
V Thiel, M Hendann, KJ Wannowius… - Journal of the American …, 2012 - ACS Publications
Grubbs–Hoveyda-type complexes with variable 4-R (complexes 1: 4-R= NEt2, O i Pr, H, F,
NO2) and 5-R substituents (complexes 2: 5-R= NEt2, O i Pr, Me, F, NO2) at the 2-isopropoxy …
NO2) and 5-R substituents (complexes 2: 5-R= NEt2, O i Pr, Me, F, NO2) at the 2-isopropoxy …
Sequence-controlled polymers through entropy-driven ring-opening metathesis polymerization: theory, molecular weight control, and monomer design
The bulk properties of a copolymer are directly affected by monomer sequence, yet efficient,
scalable, and controllable syntheses of sequenced copolymers remain a defining challenge …
scalable, and controllable syntheses of sequenced copolymers remain a defining challenge …
Stereoselective Synthesis of E,Z-Configured 1,3-Dienes by Ring-Closing Metathesis. Application to the Total Synthesis of Lactimidomycin
D Gallenkamp, A Fürstner - Journal of the American Chemical …, 2011 - ACS Publications
Strategic positioning of a silyl group on the diene unit of a diene-ene substrate allows
rigorous regio-and stereocontrol to be exerted during metathesis-based macrocyclization …
rigorous regio-and stereocontrol to be exerted during metathesis-based macrocyclization …
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 …
Mechanistic insights into the ruthenium-catalysed diene ring-closing metathesis reaction
EF Van der Eide, WE Piers - Nature chemistry, 2010 - nature.com
Ruthenium-catalysed ring-closing metathesis (RCM) is a powerful technique for the
preparation of medium-to-large rings in organic synthesis, but the details of the intimate …
preparation of medium-to-large rings in organic synthesis, but the details of the intimate …
Intramolecular C–C agostic complexes: C–C sigma interactions by another name
M Etienne, AS Weller - Chemical Society Reviews, 2014 - pubs.rsc.org
In this comprehensive review the developments in the synthesis, characterization and
reactivity of complexes (s-, d-and f-block) in which a C–C single bond interacts with a metal …
reactivity of complexes (s-, d-and f-block) in which a C–C single bond interacts with a metal …