About: Comparative investigation of ruthenium-based metathesis catalysts bearing N-heterocyclic carbene (NHC) ligands

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scientific article published on 01 August 2001

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в серпні 2001 (uk) im August 2001 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'agostu de 2001 (ast) scientific article published on 01 August 2001 (en) գիտական հոդված հրատարակված 2001 թվականի օգոստոսի 1-ին (hy)
publication date	wds:Q74448648-1827C4A3-385C-4FDF-8E61-15F9D4437FD5
publication date	2001-08-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q74448648-21762B9B-ABC7-407C-9AF5-6B6939E4F8A7 wds:Q74448648-54FD53A8-D405-49C0-B03F-3E9C3C1E21A9 wds:Q74448648-76511DB4-F386-4943-883B-BA7ADB82C65B wds:Q74448648-9B6CDDEB-8775-490E-8D65-550F7F0C508B wds:Q74448648-BBF6B9BF-7D58-4B89-8E77-0E2DF057DE2B wds:Q74448648-C08ECBE3-A158-4280-B775-2AE2249E1777 wds:Q74448648-D03ED986-4B45-444D-907F-81ED44765D72 wds:Q74448648-FADED8B2-7420-4B4D-9B7B-913535D5507E
cites work	Synthesis of Functionalized Olefins by Cross and Ring-Closing Metatheses Well-Defined Ruthenium Olefin Metathesis Catalysts: Mechanism and Activity N-Heterocyclische Carbene Stereoelectronic Effects Characterizing Nucleophilic Carbene Ligands Bound to the CpRuCl (Cp = η⁵-C₅Me₅) Moiety: A Structural and Thermochemical Investigation Influence of Sterically Demanding Carbene Ligation on Catalytic Behavior and Thermal Stability of Ruthenium Olefin Metathesis Catalysts Convenient Routes to Vinylideneruthenium Dichlorides with Basic and Bulky Tertiary Phosphine Ligands (PPrᶦ₃ and PCy₃) Simple and Convenient Synthetic Procedure Leading to Ruthenium Olefin Metathesis Catalysts Bearing the N,N‘-Bis(mesityl)imidazol-2-ylidene (IMes) Ligand Five-Coordinate 16-Electron Carbene- and Vinylideneruthenium(II) Complexes Prepared from [RuCl₂(C₈>H₁₂)]ₙ or from the New Dihydridoruthenium(IV) Compound [RuH₂Cl₂(PᶦPr₃)₂]
author name string	wds:Q74448648-12016445-844C-408F-AC79-C2302C5071D1 wds:Q74448648-345A3100-AC0A-43F7-9681-90FF1655AE06 wds:Q74448648-3FEC9CAE-782D-4711-BC75-941AD400F8CF wds:Q74448648-88E73394-BEAB-4081-B490-DC54760A4D2F wds:Q74448648-9376CAC8-E64F-4F2B-BB3D-FFA9B0EF92B4 wds:Q74448648-AE14CA65-7DA0-4705-9D65-53CFB8721B8B wds:Q74448648-CD01BA13-C096-47CC-8A72-8DDD476FA1C0 wds:Q74448648-F044BE46-CC05-44FE-A270-4E74FB68B964
author name string	R Goddard B Gabor C W Lehmann A Fürstner R Mynott F Stelzer O R Thiel L Ackermann
rdfs:label	Comparative investigation of ruthenium-based metathesis catalysts bearing N-heterocyclic carbene (nl) Comparative investigation of ruthenium-based metathesis catalysts bearing N-heterocyclic carbene (NHC) ligands (en)
skos:prefLabel	Comparative investigation of ruthenium-based metathesis catalysts bearing N-heterocyclic carbene (nl) Comparative investigation of ruthenium-based metathesis catalysts bearing N-heterocyclic carbene (NHC) ligands (en)
name	Comparative investigation of ruthenium-based metathesis catalysts bearing N-heterocyclic carbene (nl) Comparative investigation of ruthenium-based metathesis catalysts bearing N-heterocyclic carbene (NHC) ligands (en)
title	wds:Q74448648-97DCBFA1-6383-45F0-A0A7-2BA42513760A
title	Comparative investigation of ruthenium-based metathesis catalysts bearing N-heterocyclic carbene (NHC) ligands (en)
page(s)	wds:Q74448648-F6AB6520-F2A0-4F17-AE96-5610A2763BE5
page(s)	3236-3253
instance of	wds:Q74448648-168A4DA2-CDBD-4448-91D1-D0CBCD13EEED
instance of	scholarly article
PubMed ID	wds:Q74448648-99F1D9B4-0C3C-4571-858C-73ED27074E17
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11531110
PubMed ID	11531110
published in	wds:Q74448648-8EDCEA7F-167E-4BFA-B711-632DD13AC9A6
published in	Chemistry—A European Journal
issue	wds:Q74448648-358C28B7-421E-4376-B3AE-55F88BDC2FCF
volume	wds:Q74448648-D0747E35-10AE-46AC-BD83-16FDB4AF4BD4
issue	15
volume	7
DOI	wds:Q74448648-36A213A7-3C0D-48F0-833C-340630F12631
DOI	http://dx.doi.org/10.1002/1521-3765(20010803)7:15%3C3236::AID-CHEM3236%3E3.0.CO;2-S
DOI	10.1002/1521-3765(20010803)7:15<3236::AID-CHEM3236>3.0.CO;2-S
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q74448648
is cites work of	Ruthenium-based heterocyclic carbene-coordinated olefin metathesis catalysts Contemporary screening approaches to reaction discovery and development Synthesis, structure, and activity of enhanced initiators for olefin metathesis Formation of Ruthenium Carbenes by gem-Hydrogen Transfer to Internal Alkynes: Implications for Alkyne trans-Hydrogenation Formation of ruthenium carbenes by gem-hydrogen transfer to internal alkynes: implications for alkyne trans-hydrogenation Ruthenium-catalyzed ring-closing metathesis to form tetrasubstituted olefins. Fast-Initiating, Ruthenium-based Catalysts for Improved Activity in Highly E-Selective Cross Metathesis Cyclic ruthenium-alkylidene catalysts for ring-expansion metathesis polymerization Synthesis of cyclic polybutadiene via ring-opening metathesis polymerization: the importance of removing trace linear contaminants An "endless" route to cyclic polymers Salicylaldimine Ruthenium Alkylidene Complexes: Metathesis Catalysts Tuned for Protic Solvents NHC Backbone Configuration in Ruthenium-Catalyzed Olefin Metathesis Low catalyst loadings in olefin metathesis: synthesis of nitrogen heterocycles by ring-closing metathesis Backbone tuning in indenylidene-ruthenium complexes bearing an unsaturated N-heterocyclic carbene. Catalytic Kinetic Resolution of a Dynamic Racemate: Highly Stereoselective β-Lactone Formation by N-Heterocyclic Carbene Catalysis Macrocyclic poly(p-phenylenevinylene)s by ring expansion metathesis polymerisation and their characterisation by single-molecule spectroscopy. Ring-Rearrangement Metathesis (RRM) Mediated by Ruthenium-Indenylidene Complexes Towards Long-Living Metathesis Catalysts by Tuning the N-Heterocyclic Carbene (NHC) Ligand on Trifluoroacetamide-Activated Boomerang Ru Complexes A PS-DES immobilized ruthenium carbene: a robust and easily recyclable catalyst for olefin metathesis Decomposition pathways of Z-selective ruthenium metathesis catalysts Recent advances in ruthenium-based olefin metathesis Ruthenium‐Catalyzed Cyclizations: More than Just Olefin Metathesis! The Nature of the Barrier to Phosphane Dissociation from Grubbs Olefin Metathesis Catalysts Hoveyda-Grubbs catalysts with an N→Ru coordinate bond in a six-membered ring. Synthesis of stable, industrially scalable, highly efficient ruthenium metathesis catalysts and 2-vinylbenzylamine ligands as their precursors Ruthenium-based olefin metathesis catalysts with monodentate unsymmetrical NHC ligands Aqueous olefin metathesis: recent developments and applications Ruthenium-based olefin metathesis catalysts coordinated with unsymmetrical N-heterocyclic carbene ligands: synthesis, structure, and catalytic activity A Ruthenium Catalyst for Olefin Metathesis Featuring an Anti-Bredt N-Heterocyclic Carbene Ligand Ruthenium Olefin Metathesis Catalysts for the Ethenolysis of Renewable Feedstocks Grubbs and Hoveyda-Type Ruthenium Complexes Bearing a Cyclic Bent-Allene New indenylidene-type metathesis catalysts bearing unsymmetrical N-heterocyclic ligands with mesityl and nitrobenzyl substituents. Synthesis of Easy-to-Functionalize Azabicycloalkane Scaffolds as Dipeptide Turn Mimics en Route to cRGD-Based Bioconjugates The Shortest Strategy for Generating Phosphonate Prodrugs by Olefin Cross-Metathesis - Application to Acyclonucleoside Phosphonates
is cites work of	wds:Q55379648-0B6F3F2A-B04D-4996-A9E1-5549AFBED3F7

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