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Highly Efficient Ruthenium Catalysts for the Formation of Tetrasubstituted Olefins via Ring-Closing Metathesis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Synthesis of Medium-Sized Rings by the Ring-Closing Metathesis Reaction
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Recent Methods for the Synthesis of (E)‐Alkene Units in Macrocyclic Natural Products
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Multiple Metal–Carbon Bonds for Catalytic Metathesis Reactions (Nobel Lecture)
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Olefin‐Metathesis Catalysts for the Preparation of Molecules and Materials (Nobel Lecture)
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Olefin Metathesis: The Early Days (Nobel Lecture)
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Recent advances in olefin metathesis and its application in organic synthesis
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Ruthenium carbene complexes with imidazolin-2-ylidene ligands allow the formation of tetrasubstituted cycloalkenes by RCM
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The Development of L 2 X 2 RuCHR Olefin Metathesis Catalysts: An Organometallic Success Story
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Homogeneous Metathesis Polymerization by Well-Defined Group VI and Group VIII Transition-Metal Alkylidenes: Fundamentals and Applications in the Preparation of Advanced Materials
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Efficient and Recyclable Monomeric and Dendritic Ru-Based Metathesis Catalysts
inferredcites →https://doi.org/10.1021/ja048794vopenalex-snapshot
Nitro-Substituted Hoveyda−Grubbs Ruthenium Carbenes: Enhancement of Catalyst Activity through Electronic Activation
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A Recyclable Ru-Based Metathesis Catalyst
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Effects of Olefin Substitution on the Ring-Closing Metathesis of Dienes
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Improvement in Olefin Metathesis Using a New Generation of Ruthenium Catalyst Bearing an Imidazolylidene Ligand: Synthesis of Heterocycles
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Synthesis and Activity of a New Generation of Ruthenium-Based Olefin Metathesis Catalysts Coordinated with 1,3-Dimesityl-4,5-dihydroimidazol-2-ylidene Ligands
inferredcites →https://doi.org/10.1021/om060520oopenalex-snapshot
A Standard System of Characterization for Olefin Metathesis Catalysts
inferredcites →https://doi.org/10.1023/a:1019117012154openalex-snapshot
Recent advancements in ring closing olefin metathesis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Dichloro[1,3-bis(2-methylphenyl)-2-imidazolidinylidene](2-isopropoxyphenylmethylene) Ruthenium(II)
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Olefin Ring‐Closing Metathesis
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Cross metathesis of several methylenecyclopentane derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2014.05.021openalex-snapshot
Asymmetric synthesis of naturally occurring (−)-seimatopolides A and B
inferred← citeshttps://doi.org/10.1016/j.tet.2015.04.082openalex-snapshot
Applications of ring closing metathesis. Total synthesis of (±)-pseudotabersonine
inferred← citeshttps://doi.org/10.1016/j.tet.2016.06.022openalex-snapshot
Synthesis of a putative advanced intermediate en route to elisabethin A
inferred← citeshttps://doi.org/10.1016/j.tet.2018.11.047openalex-snapshot
Concise synthesis of the core structure of madreporanone by Rh-catalyzed [3+2] cycloaddition
inferred← citeshttps://doi.org/10.1016/j.tet.2019.04.060openalex-snapshot
A concise route to virginiamycin M2
inferred← citeshttps://doi.org/10.1016/j.tet.2020.131031openalex-snapshot
Strategic approaches to the synthesis of pyrrolizidine and indolizidine alkaloids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.07.161openalex-snapshot
A hexafluorobenzene promoted ring-closing metathesis to form tetrasubstituted olefins
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.09.077openalex-snapshot
Tandem cross-metathesis/hydrogenation: application to an enantioselective synthesis of pentadecyl 6-hydroxydodecanoate
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.12.060openalex-snapshot
Cross-metathesis of α-methylene-β-lactams: the first tetrasubstituted alkenes by CM
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.11.112openalex-snapshot
Acid-mediated activation of modified ring-closing metathesis catalysts
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.02.131openalex-snapshot
Strategic utilization of catalytic metathesis and photo-thermal metathesis in caged polycyclic frames
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.05.014openalex-snapshot
Synthesis of the C1–C17 fragment of the archazolids by complex cis-homodimer cross metathesis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.154102openalex-snapshot
Synthesis of (1Z)-deacylcnicin
inferred← citeshttps://doi.org/10.1016/s0959-6380(02)80009-5openalex-snapshot
Chapter 5.3 Five-membered ring systems: Furans and benzofurans
inferred← citeshttps://doi.org/10.1016/s0959-6380(09)70011-xopenalex-snapshot
Chapter 5.3: Five-membered ring systems: furans and benzofurans
inferred← citeshttps://doi.org/10.1021/acs.biomac.5c02116openalex-snapshot
The Impact of Structure Refinement in the Construction of Whole-Cell Catalysts with Artificial Metalloenzymes Assembled in Artificial Sanctuaries
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.9b01887openalex-snapshot
Synthesis of Novel Potent Archazolids: Pharmacology of an Emerging Class of Anticancer Drugs
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00128openalex-snapshot
Large Macrocyclic Lactones as Specific Cuticular Lipids of Eueides Butterflies
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02821openalex-snapshot
Divinylcarbinol Desymmetrization Strategy: A Concise and Reliable Approach to Chiral Hydroxylated Fatty Acid Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00946openalex-snapshot
Modular Total Synthesis of iso-Archazolids and Archazologs
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00659openalex-snapshot
Ring-Closing Enyne Metathesis of Terminal Alkynes with Propargylic Hindrance
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01844openalex-snapshot
Asymmetric Total Synthesis of the Indole Diterpene Alkaloid Paspaline
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02473openalex-snapshot
Phosphate Tether-Mediated Ring-Closing Metathesis for the Generation of P-Stereogenic, Z-Configured Bicyclo[7.3.1]- and Bicyclo[8.3.1]phosphates
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02581openalex-snapshot
A General Route to β-Substituted Pyrroles by Transition-Metal Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00383openalex-snapshot
Total Synthesis of (+)-Ansatrienol K
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01302openalex-snapshot
Diastereoselective Ring-Closing Metathesis as a Means to Construct Medium-Sized Cyclic Ethers: Application to the Synthesis of a Photoactivatable Gambierol Derivative
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02208openalex-snapshot
Elaboration of Sterically Hindered δ-Lactones through Ring-Closing Metathesis: Application to the Synthesis of the C1–C27 Fragment of Hemicalide
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02458openalex-snapshot
Short Enantioselective Total Syntheses of Cheloviolenes A and B and Dendrillolide C via Convergent Fragment Coupling Using a Tertiary Carbon Radical
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00415openalex-snapshot
Synthesis of gem-Difluoromethylene Containing Cycloalkenes via the Ring-Opening Reaction of gem-Difluorocyclopropanes and Subsequent RCM Reaction
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02268openalex-snapshot
Synthesis of Functionalized 6,5- and 7,5-Azabicycloalkane Amino Acids by Metathesis Reactions
inferred← citeshttps://doi.org/10.1021/acs.macromol.3c01146openalex-snapshot
Encapsulated Transition Metal Catalysts Enable Long-term Stability in Frontal Polymerization Resins
inferred← citeshttps://doi.org/10.1021/acs.macromol.4c00972openalex-snapshot
Polymerization of Free-Volume-Promoting Monomers for Methane Absorption
inferred← citeshttps://doi.org/10.1021/acs.macromol.5b01058openalex-snapshot
Ru-Catalyzed Isomerization Provides Access to Alternating Copolymers via Ring-Opening Metathesis Polymerization
inferred← citeshttps://doi.org/10.1021/acs.macromol.5b02067openalex-snapshot
New Synthetic Approach for Optically Active Polymer Bearing Chiral Cyclic Architecture: Combination of Asymmetric Allylic Amidation and Ring-Closing Metathesis Reaction
inferred← citeshttps://doi.org/10.1021/acs.oprd.6b00167openalex-snapshot
Highlights of the Recent U.S. Patent Literature: Focus on Metathesis
inferred← citeshttps://doi.org/10.1021/acs.oprd.8b00093openalex-snapshot
Ring-Closing Metathesis in Pharmaceutical Development: Fundamentals, Applications, and Future Directions
inferred← citeshttps://doi.org/10.1021/acs.organomet.5b00715openalex-snapshot
Variation of the Sterical Properties of the N-Heterocyclic Carbene Coligand in Thermally Triggerable Ruthenium-Based Olefin Metathesis Precatalysts/Initiators
inferred← citeshttps://doi.org/10.1021/acs.organomet.7b00677openalex-snapshot
Light- and Thermal-Activated Olefin Metathesis of Hindered Substrates
inferred← citeshttps://doi.org/10.1021/acs.organomet.8b00041openalex-snapshot
Conformational Control of Initiation Rate in Hoveyda–Grubbs Precatalysts
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01344openalex-snapshot
Ruthenium Metathesis: A Key Step To Access a New Cyclic Tetrasubstituted Olefin Platform
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03806openalex-snapshot
Intramolecular Sakurai Allylation of Geminal Bis(silyl) Enamide with Indolenine. A Diastereoselective Cyclization To Form Functionalized Hexahydropyrido[3,4-b]Indole
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04846openalex-snapshot
Ring-Closing Metathesis for Fluoroolefins Using Ruthenium Catalysts with Six-Membered NHC Ligands
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b03138openalex-snapshot
Synthesis of Denosomin–Vitamin D3 Hybrids and Evaluation of Their Anti-Alzheimer’s Disease Activities
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02962openalex-snapshot
A Second-Generation Synthesis of the Cyanthiwigin Natural Product Core
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03979openalex-snapshot
Enantioselective, Protecting-Group-Free Total Synthesis of Boscartin F
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03715openalex-snapshot
Total Synthesis of Archazolid F
inferred← citeshttps://doi.org/10.1021/acscatal.0c02770openalex-snapshot
Sterically Tuned N -Heterocyclic Carbene Ligands for the Efficient Formation of Hindered Products in Ru-Catalyzed Olefin Metathesis
inferred← citeshttps://doi.org/10.1021/acscatal.8b00843openalex-snapshot
An Initiation Kinetics Prediction Model Enables Rational Design of Ruthenium Olefin Metathesis Catalysts Bearing Modified Chelating Benzylidenes
inferred← citeshttps://doi.org/10.1021/acssuschemeng.6b01648openalex-snapshot
Toward Sustainable Synthesis of PA12 (Nylon-12) Precursor from Oleic Acid Using Ring-Closing Metathesis
inferred← citeshttps://doi.org/10.1021/ci4007497openalex-snapshot
Automated Design of Realistic Organometallic Molecules from Fragments
inferred← citeshttps://doi.org/10.1021/cr800524fopenalex-snapshot
Ruthenium-Based Olefin Metathesis Catalysts Bearing N-Heterocyclic Carbene Ligands
inferred← citeshttps://doi.org/10.1021/cr9002424openalex-snapshot
Ruthenium-Based Heterocyclic Carbene-Coordinated Olefin Metathesis Catalysts
inferred← citeshttps://doi.org/10.1021/cs300580gopenalex-snapshot
Exo/endo Selectivity of the Ring-Closing Enyne Methathesis Catalyzed by Second Generation Ru-Based Catalysts. Influence of Reactant Substituents
inferred← citeshttps://doi.org/10.1021/cs500539mopenalex-snapshot
Operation of the Boomerang Mechanism in Olefin Metathesis Reactions Promoted by the Second-Generation Hoveyda Catalyst
inferred← citeshttps://doi.org/10.1021/ic901444copenalex-snapshot
Predicting the Cis−Trans Dichloro Configuration of Group 15−16 Chelated Ruthenium Olefin Metathesis Complexes: A DFT and Experimental Study
inferred← citeshttps://doi.org/10.1021/ja075849vopenalex-snapshot
Synthesis and Activity of Ruthenium Olefin Metathesis Catalysts Coordinated with Thiazol-2-ylidene Ligands
inferred← citeshttps://doi.org/10.1021/ja1029045openalex-snapshot
Nonproductive Events in Ring-Closing Metathesis Using Ruthenium Catalysts
inferred← citeshttps://doi.org/10.1021/ja202012sopenalex-snapshot
Control of Olefin Geometry in Macrocyclic Ring-Closing Metathesis Using a Removable Silyl Group
inferred← citeshttps://doi.org/10.1021/ja2031085openalex-snapshot
Stereoselective Synthesis ofE,Z-Configured 1,3-Dienes by Ring-Closing Metathesis. Application to the Total Synthesis of Lactimidomycin
inferred← citeshttps://doi.org/10.1021/ja305856qopenalex-snapshot
Total Synthesis of (−)-Isoschizogamine
inferred← citeshttps://doi.org/10.1021/ja4025963openalex-snapshot
Studies on the Himbert Intramolecular Arene/Allene Diels–Alder Cycloaddition. Mechanistic Studies and Expansion of Scope to All-Carbon Tethers
inferred← citeshttps://doi.org/10.1021/ja409618popenalex-snapshot
Computation and Experiment Reveal That the Ring-Rearrangement Metathesis of Himbert Cycloadducts Can Be Subject to Kinetic or Thermodynamic Control
inferred← citeshttps://doi.org/10.1021/ja710294kopenalex-snapshot
The Catalytic Asymmetric Total Synthesis of Elatol
inferred← citeshttps://doi.org/10.1021/ja800861popenalex-snapshot
Identification and Characterization of a New Family of Catalytically Highly Active Imidazolin-2-ylidenes
inferred← citeshttps://doi.org/10.1021/ja8078913openalex-snapshot
Conformations of N-Heterocyclic Carbene Ligands in Ruthenium Complexes Relevant to Olefin Metathesis
inferred← citeshttps://doi.org/10.1021/ja900067copenalex-snapshot
Effects of NHC-Backbone Substitution on Efficiency in Ruthenium-Based Olefin Metathesis
inferred← citeshttps://doi.org/10.1021/ja909441xopenalex-snapshot
Flexibility of N-Heterocyclic Carbene Ligands in Ruthenium Complexes Relevant to Olefin Metathesis and Their Impact in the First Coordination Sphere of the Metal
inferred← citeshttps://doi.org/10.1021/jacs.3c07019openalex-snapshot
Streamlined Strategy for Scalable and Enantioselective Total Syntheses of the Eburnane Alkaloids
inferred← citeshttps://doi.org/10.1021/jacs.3c10826openalex-snapshot
Latency for All: Enabling Latency of Hoveyda–Grubbs Second-Generation Catalysts by Adding Phosphite Ligands
inferred← citeshttps://doi.org/10.1021/jacs.4c16900openalex-snapshot
Enantioselective Total Syntheses of Vallesamidine and Schizozygane Alkaloids
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