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Structural analogues of Hoveyda–Grubbs catalysts bearing the 1-benzofuran moiety or isopropoxy-1-benzofuran derivatives as olefin metathesis catalysts
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The 50 checked references that resolve
resolves10.1016/S0040-4039(99)00217-8
Increased ring closing metathesis activity of ruthenium-based olefin metathesis catalysts coordinated with imidazolin-2-ylidene ligands
resolves10.1021/ja9831352
Olefin Metathesis-Active Ruthenium Complexes Bearing a Nucleophilic Carbene Ligand
resolves10.1021/om990788y
Influence of Sterically Demanding Carbene Ligation on Catalytic Behavior and Thermal Stability of Ruthenium Olefin Metathesis Catalysts
resolves10.1021/ja001179g
Efficient and Recyclable Monomeric and Dendritic Ru-Based Metathesis Catalysts
resolves10.1021/cr9002424
Ruthenium-Based Heterocyclic Carbene-Coordinated Olefin Metathesis Catalysts
resolves10.1021/cr800524f
Ruthenium-Based Olefin Metathesis Catalysts Bearing <i>N</i>-Heterocyclic Carbene Ligands
resolves10.1038/nature14061
High-value alcohols and higher-oxidation-state compounds by catalytic Z-selective cross-metathesis
resolves10.1002/anie.201302724
Alkene Chemoselectivity in Ruthenium‐Catalyzed <i>Z</i>‐Selective Olefin Metathesis
resolves10.1039/C3GC41943F
An attempt to provide an environmentally friendly solvent selection guide for olefin metathesis
resolves10.1016/S0960-894X(02)00260-3
A solid-Supported phosphine-Free ruthenium alkylidene for olefin metathesis in methanol and water
resolves10.1039/C1DT11404B
Chelating alkylidene ligands as pacifiers for ruthenium catalysed olefinmetathesis
resolves10.1021/jacs.5b01144
Origins of Initiation Rate Differences in Ruthenium Olefin Metathesis Catalysts Containing Chelating Benzylidenes
resolves10.1002/adsc.200600478
Probing of the Ligand Anatomy: Effects of the Chelating Alkoxy Ligand Modifications on the Structure and Catalytic Activity of Ruthenium Carbene Complexes
resolves10.1021/ja048794v
Nitro-Substituted Hoveyda−Grubbs Ruthenium Carbenes: Enhancement of Catalyst Activity through Electronic Activation
resolves10.1021/acs.joc.5b01091
Divergent Approach to a Family of Tyrosine-Derived Ru–Alkylidene Olefin Metathesis Catalysts
resolves10.1016/j.jorganchem.2010.02.025
New efficient ruthenium metathesis catalyst containing chromenyl ligand
resolves10.1071/CH08443
Hindered Rotation in New Air-Stable Ruthenium Olefin Metathesis Catalysts with Chromanylmethylidene Ligands
resolves10.1016/j.jorganchem.2011.12.024
New nitrochromenylmethylidene-containing ruthenium metathesis catalyst
resolves10.1007/s00044-008-9149-5
Synthesis of new derivatives of 2,2-dimethyl-2,3-dihydro-7-benzo[b]furanol with potential antimicrobial activity
resolves10.1124/jpet.112.196980
Synthesis and Antifungal Activity of Derivatives of 2- and 3-Benzofurancarboxylic Acids
resolves10.1007/s00706-013-1067-7
Microwave-assisted preparation and antimicrobial activity of O-alkylamino benzofurancarboxylates
resolves10.1007/s11224-012-9959-4
Derivatives of benzo[b]furan. Part I. Conformational studies of khellinone and visnaginone
resolves10.1016/j.cplett.2013.01.011
Two coordination modes around the Cu(II) cations in complexes with benzo[b]furancarboxylic acids
resolves10.1016/j.cplett.2014.06.063
The activation mechanism of Fe-based olefin metathesis catalysts
resolves10.1039/c3dt32884h
Exploring new generations of ruthenium olefin metathesis catalysts: the reactivity of a bis-ylidene ruthenium complex by DFT
resolves10.1039/C5DT03446A
Nitrenium ions and trivalent boron ligands as analogues of N-heterocyclic carbenes in olefin metathesis: a computational study
resolves10.1021/ja300865u
An Evolutionary Algorithm for <i>de Novo</i> Optimization of Functional Transition Metal Compounds
resolves10.1039/b815665d
Relevance of cis- and trans-dichloride Ru intermediates in Grubbs-II olefin metathesis catalysis (H2IMesCl2RuCHR)
resolves10.1021/om500315t
Impact of Electronic Modification of the Chelating Benzylidene Ligand in <i>cis</i>-Dichloro-Configured Second-Generation Olefin Metathesis Catalysts on Their Activity
resolves10.1021/ic901444c
Predicting the <i>Cis−Trans</i> Dichloro Configuration of Group 15−16 Chelated Ruthenium Olefin Metathesis Complexes: A DFT and Experimental Study
resolves10.1021/om5006462
Conformational Flexibility of Hoveyda-Type and Grubbs-Type Complexes Bearing Acyclic Carbenes and Its Impact on Their Catalytic Properties
resolves10.1021/om200529m
Carbene Rotamer Switching Explains the Reverse Trans Effect in Forming the Grubbs Second-Generation Olefin Metathesis Catalyst
resolves10.1039/c1cc11230a
What is the initiation step of the Grubbs-Hoveyda olefinmetathesiscatalyst?
resolves10.1002/ange.201000581
Probing the Mechanism of Olefin Metathesis in Grubbs–Hoveyda and Grela Type Complexes
resolves10.1002/chem.200800704
Is the Hoveyda–Grubbs Complex a Vinylogous Fischer‐Type Carbene? Aromaticity‐Controlled Activity of Ruthenium Metathesis Catalysts
resolves10.1016/S0040-4020(03)01075-5
Benzene fused five-membered heterocycles. A theoretical approach
resolves10.1021/ct5003863
The Right Computational Recipe for Olefin Metathesis with Ru-Based Catalysts: The Whole Mechanism of Ring-Closing Olefin Metathesis
resolves10.1021/om301192a
Complete Reaction Pathway of Ruthenium-Catalyzed Olefin Metathesis of Ethyl Vinyl Ether: Kinetics and Mechanistic Insight from DFT
resolves10.1021/om400064c
3-Bromopyridine As a Sixth Ligand in Sulfoxide-Based Hoveyda Complexes: A Study on Catalytic Properties
resolves10.1021/om400233s
Structural and Mechanistic Basis of the Fast Metathesis Initiation by a Six-Coordinated Ruthenium Catalyst
resolves10.1039/c1cp20834a
Validation of electronic structure methods for isomerization reactions of large organic molecules
resolves10.1021/acs.jpclett.5b01591
Treating London-Dispersion Effects with the Latest Minnesota Density Functionals: Problems and Possible Solutions
resolves10.1080/00268977000101561
The calculation of small molecular interactions by the differences of separate total energies. Some procedures with reduced errors
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