In an attempt to provide a user's guide to the galaxy of benzylidene, alkoxybenzylidene, and indenylidene ruthenium olefin metathesis catalysts.
about
Olefin metathesis in airRing-closing metathesis reactions: interpretation of conversion-time data.Pulsed-addition ring-opening metathesis polymerization: catalyst-economical syntheses of homopolymers and block copolymers.Reactivation of a Ruthenium-Based Olefin Metathesis Catalyst.Metathesis access to monocyclic iminocyclitol-based therapeutic agents.DFT mechanistic study on diene metathesis catalyzed by Ru-based Grubbs-Hoveyda-type carbenes: the key role of pi-electron density delocalization in the Hoveyda ligand.Evolution of catalytic stereoselective olefin metathesis: from ancillary transformation to purveyor of stereochemical identity.About the activity and selectivity of less well-known metathesis catalysts during ADMET polymerizations.Cross-metathesis of allylcarboranes with O-allylcyclodextrins.Halide exchanged Hoveyda-type complexes in olefin metathesisLight-induced olefin metathesis.Backbone tuning in indenylidene-ruthenium complexes bearing an unsaturated N-heterocyclic carbene.Effects of NHC-backbone substitution on efficiency in ruthenium-based olefin metathesis.Design and stereoselective preparation of a new class of chiral olefin metathesis catalysts and application to enantioselective synthesis of quebrachamine: catalyst development inspired by natural product synthesis.Toward a simulation approach for alkene ring-closing metathesis: scope and limitations of a model for RCM.Computational study of productive and non-productive cycles in fluoroalkene metathesis.Low catalyst loadings in olefin metathesis: synthesis of nitrogen heterocycles by ring-closing metathesisConsequences of the electronic tuning of latent ruthenium-based olefin metathesis catalysts on their reactivity.Formation of a dicationic ruthenium benzyl complex by halide abstraction from a Grubbs-type second-generation benzylidene.Assessing the ligand properties of 1,3-dimesitylbenzimidazol-2-ylidene in ruthenium-catalyzed olefin metathesis.Batchwise and continuous nanofiltration of POSS-tagged Grubbs-Hoveyda-type olefin metathesis catalysts.Role of grafted alkoxybenzylidene ligand in silica-supported Hoveyda-Grubbs-type catalysts.Forged and fashioned for faithfulness-ruthenium olefin metathesis catalysts bearing ammonium tags.Ruthenium Catalysts Supported by Amino-Substituted N-Heterocyclic Carbene Ligands for Olefin Metathesis of Challenging Substrates.Tube-in-tube reactor as a useful tool for homo- and heterogeneous olefin metathesis under continuous flow mode.Ruthenium-Amido Complexes: Synthesis, Structure, and Catalytic Activity in Olefin MetathesisSynthesis of Stable Ruthenium Olefin Metathesis Catalysts with Mixed Anionic LigandsThe Doping Effect of Fluorinated Aromatic Solvents on the Rate of Ruthenium-Catalysed Olefin MetathesisContinuous flow ring-closing metathesis, an environmentally-friendly route to 2,5-dihydro-1H-pyrrole-3-carboxylatesRenewable materials as precursors of linear nitrile-acid derivatives viacross-metathesis of fatty esters and acids with acrylonitrile and fumaronitrile
P2860
Q26776196-3EEFE6B9-18D9-459E-BC32-90838027A31EQ30677846-AE899890-77D3-4AA9-9794-3BD8B56D252AQ33408930-9AF348D5-28D1-4D4C-AD92-8282BCEC2C29Q36552002-FA1E25BB-D2A5-40F1-B109-AD94BF3535C7Q37909033-94591577-7C15-484A-9EEA-BB570B3F31F6Q39874188-A93FA155-D541-420F-8675-12445AB727D2Q40433430-9A428202-D6F3-4C4F-9A5B-47E4336BB729Q41155784-3FC4D679-221A-43A6-BCB2-151234B4A842Q41156025-BB68525C-98F3-4767-B7CB-FE7DEB566A10Q41156828-6EDFA0E7-50C8-4FA8-86B0-036BB39E0918Q41157838-F754D69E-755E-42A2-8AAA-EC868AE2D61AQ41158415-F6AF6325-1350-4898-AE72-1456B4868327Q41815479-2FA9923B-6B73-4F7D-B24B-CB8E818ACC19Q41851846-9E730645-526D-4526-8CBA-E64113AFB47AQ41862624-49CD04F4-16C1-42EB-9305-AC8951656E0BQ41991523-EA569842-0731-4EE2-9D5A-600C19040D19Q42200967-162CBA58-2955-477A-B68E-3161D0A731C7Q42585500-09773A52-69E2-4267-97E9-50AB9ED0682BQ45031612-7D4E49B7-7EB3-486B-995C-49D9433AC8C9Q45399920-C431D30B-788F-4876-A77D-E8A3B54A8BB7Q45796217-9CB0F756-BD1D-4137-8B9E-EBFC2F85684EQ46808820-CE607899-CB42-4FE7-992A-079F8D479017Q47776367-C18BCE8F-3182-4449-8D97-0FF89566F81EQ48181888-1E5245F4-9720-4566-8C7F-2DE4FE903FBAQ54684252-92965022-F4AF-41AA-A732-0B657DCDAF89Q57945147-E3647140-D32E-483C-890F-56911D3C8A31Q57945153-52B95C30-CFDD-48A7-A1AE-40EBF0361DA7Q57945209-969C9D67-9BB2-44B4-88B8-86BE21C6FD08Q58099218-2106FE5C-AFCC-44A0-ABE7-C708CE2AFCA2Q58382164-6414B169-BEC0-4D12-B946-59801BF47E5D
P2860
In an attempt to provide a user's guide to the galaxy of benzylidene, alkoxybenzylidene, and indenylidene ruthenium olefin metathesis catalysts.
description
2008 nî lūn-bûn
@nan
2008 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
In an attempt to provide a use ...... m olefin metathesis catalysts.
@ast
In an attempt to provide a use ...... m olefin metathesis catalysts.
@en
In an attempt to provide a use ...... m olefin metathesis catalysts.
@nl
type
label
In an attempt to provide a use ...... m olefin metathesis catalysts.
@ast
In an attempt to provide a use ...... m olefin metathesis catalysts.
@en
In an attempt to provide a use ...... m olefin metathesis catalysts.
@nl
prefLabel
In an attempt to provide a use ...... m olefin metathesis catalysts.
@ast
In an attempt to provide a use ...... m olefin metathesis catalysts.
@en
In an attempt to provide a use ...... m olefin metathesis catalysts.
@nl
P356
P1476
In an attempt to provide a use ...... um olefin metathesis catalysts
@en
P2093
Anna Michrowska
Michał Bieniek
P304
P356
10.1002/CHEM.200701340
P407
P577
2008-01-01T00:00:00Z