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Principaux documents

687944

Sigma-Aldrich

Ruthenium Metathesis Catalysts Kit I

Synonyme(s) :

Ruthenium Metathesis Catalysts

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About This Item

Code UNSPSC :
12352300
Nomenclature NACRES :
NA.22

Pertinence de la réaction

core: ruthenium
reagent type: catalyst
reaction type: Ring-Opening Polymerization

Température de stockage

2-8°C

Application

Metathesis: Ruthenium-Based Metathesis Catalysts
Metathesis: Ruthenium-Based Metathesis Catalysts
Ruthenium metathesis catalysts kit I consists of 9 samples of Grubbs 1st and 2nd generation catalysts. These catalysts have applications in ring-closing and ring-opening metathesis, cross-metathesis, ring-opening metathesis polymerization (ROMP) and enyne metathesis.

Autres remarques

Grubbs Catalyst® Technology for Olefin Metathesis by Aldrich

Informations légales

Each individual catalyst contained in this product is subject to one or more US patents and associated foreign equivalents thereof. This product includes a limited one-time, non-exclusive, non-transferable license to use the Product for research purposes only. It is the sole responsibility of buyer to ensure that its use of the product does not infringe the rights of others. For questions, please contact us at aldrich@sial.com
Grubbs Catalyst is a registered trademark of Umicore AG & Co. KG

Composants de kit également disponibles séparément

Réf. du produit
Description
FDS
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  • 569755Hoveyda-Grubbs Catalyst® M720, Umicore, 97% 100 mgFDS
  • 577944Hoveyda-Grubbs Catalyst® M700, Umicore 100 mgFDS
  • 682284Grubbs Catalyst® M205, Umicore 100 mgFDS
  • 682330Grubbs Catalyst® M300 100 mgFDS
  • 682365Grubbs Catalyst® M207, Umicore 100 mgFDS
  • 682373Hoveyda-Grubbs Catalyst® M721, Umicore 100 mgFDS
  • 682381Grubbs Catalyst® M360 100 mgFDS
Afficher tout (9)

Code de la classe de stockage

12 - Non Combustible Liquids

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

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Certificats d'analyse (COA)

Lot/Batch Number

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Enyne metathesis (enyne bond reorganization)
Diver, ST and Giessert, A
Chemical Reviews, 104(3), 1317-1382 (2004)
Controlled Living Ring-Opening-Metathesis Polymerization by a Fast-Initiating Ruthenium Catalyst
Choi, T and Grubbs, RH
Angewandte Chemie (International ed. in English), 42(15), 1743-1746 (2003)
A general model for selectivity in olefin cross metathesis
Chatterjee, AK et al.
Journal of the American Chemical Society, 125(37), 11360-11370 (2003)
The total synthesis of (+)-migrastatin.
Gaul C, et al.
Journal of the American Chemical Society, 125(20), 6042-6043 (2003)
T M Trnka et al.
Accounts of chemical research, 34(1), 18-29 (2001-02-15)
In recent years, the olefin metathesis reaction has attracted widespread attention as a versatile carbon-carbon bond-forming method. Many new applications have become possible because of major advances in catalyst design. State-of-the-art ruthenium catalysts are not only highly active but also
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