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Sigma-Aldrich

Ruthenium Metathesis Catalysts Kit I

Sinónimos:

Ruthenium Metathesis Catalysts

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About This Item

Código UNSPSC:
12352300
NACRES:
NA.22

idoneidad de la reacción

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

temp. de almacenamiento

2-8°C

Aplicación

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.

Otras notas

Grubbs Catalyst® Technology for Olefin Metathesis by Aldrich

Información legal

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 [email protected]
Grubbs Catalyst is a registered trademark of Umicore AG & Co. KG

Los componentes del kit también están disponibles por separado

Referencia del producto
Descripción
SDS
  • 579726Grubbs Catalyst® M102, Umicore, 97% 1 gSDS
  • 569747Grubbs Catalyst® M204, Umicore 100 mgSDS
  • 569755Hoveyda-Grubbs Catalyst® M720, Umicore, 97% 100 mgSDS
  • 577944Hoveyda-Grubbs Catalyst® M700, Umicore 100 mgSDS
  • 682284Grubbs Catalyst® M205, Umicore 100 mgSDS
  • 682330Grubbs Catalyst® M300 100 mgSDS
  • 682365Grubbs Catalyst® M207, Umicore 100 mgSDS
  • 682373Hoveyda-Grubbs Catalyst® M721, Umicore 100 mgSDS
  • 682381Grubbs Catalyst® M360 100 mgSDS
Ver todo (9)

Código de clase de almacenamiento

12 - Non Combustible Liquids

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

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Certificados de análisis (COA)

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A general model for selectivity in olefin cross metathesis
Chatterjee, AK et al.
Journal of the American Chemical Society, 125(37), 11360-11370 (2003)
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)
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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Grubbs Group – Prof. Product Portal

Research focuses on ruthenium alkylidene complexes for versatile olefin metatheses catalysis in the Grubbs group.

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