Literature DB >> 18064624

In an attempt to provide a user's guide to the galaxy of benzylidene, alkoxybenzylidene, and indenylidene ruthenium olefin metathesis catalysts.

Michał Bieniek1, Anna Michrowska, Dmitry L Usanov, Karol Grela.   

Abstract

The data reported in this paper demonstrate that great care must be taken when choosing an appropriate catalyst for a given metathesis reaction. First-generation catalysts were found to be useful in the metathesis of sterically unhindered substrates. Second-generation catalysts (under optimised conditions) showed good to excellent activities toward sterically hindered and electron-withdrawing group (EWG)-substituted alkenes that do not react using the first-generation complexes. A strong temperature effect was noted on all of the reactions tested. Interestingly, attempts to force a reaction by increasing the catalyst loading were much less effective. Therefore, when possible, it is suggested that metathesis transformations should be carried out with a second-generation catalyst at 70 degrees C in toluene. However, different second-generation catalysts proved to be optimal for different applications and no single catalyst outperformed all others in all cases. Nevertheless, some empirical rules can be deduced from the model experiments, providing preliminary hints for the selection of the optimal catalysts.

Entities:  

Year:  2008        PMID: 18064624     DOI: 10.1002/chem.200701340

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  20 in total

1.  Recent advances in the application of ring-closing metathesis for the synthesis of unsaturated nitrogen heterocycles.

Authors:  Emilia J Groso; Corinna S Schindler
Journal:  Synthesis (Stuttg)       Date:  2019-02-08       Impact factor: 3.157

2.  Low catalyst loadings in olefin metathesis: synthesis of nitrogen heterocycles by ring-closing metathesis.

Authors:  Kevin M Kuhn; Timothy M Champagne; Soon Hyeok Hong; Wen-Hao Wei; Andrew Nickel; Choon Woo Lee; Scott C Virgil; Robert H Grubbs; Richard L Pederson
Journal:  Org Lett       Date:  2010-03-05       Impact factor: 6.005

3.  Pulsed-addition ring-opening metathesis polymerization: catalyst-economical syntheses of homopolymers and block copolymers.

Authors:  John B Matson; Scott C Virgil; Robert H Grubbs
Journal:  J Am Chem Soc       Date:  2009-03-11       Impact factor: 15.419

4.  Effects of NHC-backbone substitution on efficiency in ruthenium-based olefin metathesis.

Authors:  Kevin M Kuhn; Jean-Baptiste Bourg; Cheol K Chung; Scott C Virgil; Robert H Grubbs
Journal:  J Am Chem Soc       Date:  2009-04-15       Impact factor: 15.419

5.  Reactivation of a Ruthenium-Based Olefin Metathesis Catalyst.

Authors:  Daniel S Tabari; Daniel R Tolentino; Yann Schrodi
Journal:  Organometallics       Date:  2012-12-21       Impact factor: 3.876

6.  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.

Authors:  Elizabeth S Sattely; Simon J Meek; Steven J Malcolmson; Richard R Schrock; Amir H Hoveyda
Journal:  J Am Chem Soc       Date:  2009-01-28       Impact factor: 15.419

7.  Toward a simulation approach for alkene ring-closing metathesis: scope and limitations of a model for RCM.

Authors:  David J Nelson; Davide Carboni; Ian W Ashworth; Jonathan M Percy
Journal:  J Org Chem       Date:  2011-09-27       Impact factor: 4.354

8.  About the activity and selectivity of less well-known metathesis catalysts during ADMET polymerizations.

Authors:  Hatice Mutlu; Lucas Montero de Espinosa; Oĝuz Türünç; Michael A R Meier
Journal:  Beilstein J Org Chem       Date:  2010-12-03       Impact factor: 2.883

9.  Cross-metathesis of allylcarboranes with O-allylcyclodextrins.

Authors:  Ivan Snajdr; Zbyněk Janoušek; Jindřich Jindřich; Martin Kotora
Journal:  Beilstein J Org Chem       Date:  2010-11-23       Impact factor: 2.883

10.  Backbone tuning in indenylidene-ruthenium complexes bearing an unsaturated N-heterocyclic carbene.

Authors:  César A Urbina-Blanco; Xavier Bantreil; Hervé Clavier; Alexandra M Z Slawin; Steven P Nolan
Journal:  Beilstein J Org Chem       Date:  2010-11-23       Impact factor: 2.883

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