Grubbs Catalyst® M102

Dichloro(benzylidene)bis(tricyclohexylphosphine)ruthenium(II)

CAS Number: 172222-30-9

Your contact person

Yukari Nakada

T: +81 90 9018 6731

Chinmay Pandya

T: +91 9867662944

Don Zeng

T: +1 (714) 777 3737

Heidi Heuser

T: +49 6181 706 4787

Ula Rao

T: +86 (21) 2411 6843

Heidi Heuser

T: +49 6181 706 4787

Please order your research quantities at Merck / MilliporeSigma

Order sample

Applications & references

Description

Formal Synthesis of (-)-Haliclonin A: Stereoselective Construction of an Azabicyclo[3.3.1]nonane Ring System by a Tandem Radical Reaction.

Reference: Org. Lett. 2020, 22, 13, 5046–5050

Formylation of a metathesis-derived ansa[4]-ferrocene: a simple route to anticancer organometallics.

Reference: Dalton Trans. 2020, (doi.org/10.1039/D0DT01975E)

Aerogels for the separation of asphalt-containing oil–water mixtures and the effect of asphalt stabilizer.

Reference: RSC Adv. 2020,10, 24840-24846

Asymmetric total synthesis of the naturally occurring antibiotic Anthracimycin

Reference: Org. Lett. 2020, 22, 14, 5550–5554

Sequential two-fold Claisen Rearrangement, One-pot Ring Closing Metathesis and Cross-metathesis as a Route to Substituted Benzo[b]azepine-2-one, Benzo[b]azepine and Benzo[b]oxepine Derivatives.

Reference: Helv Chem Acta 2020 ASAP (doi.org/10.1002/hlca.202000216)

Grubbs Catalyst® M102

Grubbs Catalyst® M102

Dichloro(benzylidene)bis(tricyclohexylphosphine)ruthenium(II)

Chemical properties

Your contact person

Yukari Nakada

Chinmay Pandya

Don Zeng

Heidi Heuser

Ula Rao

Heidi Heuser

Please order your research quantities at Merck / MilliporeSigma

Applications & references

Description

Formal Synthesis of (-)-Haliclonin A: Stereoselective Construction of an Azabicyclo[3.3.1]nonane Ring System by a Tandem Radical Reaction.

Formylation of a metathesis-derived ansa[4]-ferrocene: a simple route to anticancer organometallics.

Aerogels for the separation of asphalt-containing oil–water mixtures and the effect of asphalt stabilizer.

Asymmetric total synthesis of the naturally occurring antibiotic Anthracimycin

Sequential two-fold Claisen Rearrangement, One-pot Ring Closing Metathesis and Cross-metathesis as a Route to Substituted Benzo[b]azepine-2-one, Benzo[b]azepine and Benzo[b]oxepine Derivatives.

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