Issue 9, 2000

Cross-metathesis [italic v (to differentiate from Times ital nu)]s. silylative coupling of vinyl alkyl ethers with vinylsilanes catalyzed by a ruthenium–carbene complex (Grubbs catalyst)

Abstract

Grubbs complex, (PCy3)2Cl2Ru[double bond, length half m-dash]CHPh (I) is a very effective catalyst of the cross-disproportionation of vinyl-trisubstituted silanes H2C[double bond, length half m-dash]CHSiR3 [where R3=Me3, PhMe2, (OEt)3] with vinyl alkyl ethers H2C[double bond, length half m-dash]CHOR′ [where R′=ethyl, propyl, butyl, t-butyl, t-pentyl, 2-(ethyl)hexyl, cyclohexyl, trimethylsilyl] to yield a mixture of (E+Z) 1-silyl-2-alkoxyethenes. The reaction occurs quantitatively under milder conditions (60°C) than the analogous one catalyzed by Ru–H and/or Ru–Si complexes reported previously (80°C). The stoichiometric reaction of (I) and (PCy3)2Cl2Ru[double bond, length half m-dash]CH2 (III) with vinyl ethyl ether leads to the formation of (PCy3)2Cl2Ru[double bond, length half m-dash]CH(OEt) (II), inactive in the stoichiometric reaction with vinylsilanes but very active in the catalytic process. Experiments with the use of deuterated vinylsilanes indicate the non-metallacarbene mechanism of the reaction and provide evidence for the initiation of Ru–H bond formation [italic v (to differentiate from Times ital nu)]ia the hydrovinylation with vinylsilanes.

Article information

Article type
Paper
Submitted
26 Apr 2000
Accepted
30 Jun 2000
First published
17 Aug 2000

New J. Chem., 2000,24, 671-675

Cross-metathesis [italic v (to differentiate from Times ital nu)]s. silylative coupling of vinyl alkyl ethers with vinylsilanes catalyzed by a ruthenium–carbene complex (Grubbs catalyst)

B. Marciniec, M. Kujawa and C. Pietraszuk, New J. Chem., 2000, 24, 671 DOI: 10.1039/B003442H

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements