Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Grubb

Internationally renowned authors, among them K. C. Nicolaou, H. Iwamura, R. H. Grubbs and H. Hopf, present the full potential of acetylene chemistry, from organic synthesis through materials science to bioorganic chemistry. [Pg.799]

Grubbs, R., Risse, W. and Novae, B. The Development of Well-defined Catalysts for Ring-Opening Olefin Metathesis. Vol. 102, pp. 47-72. [Pg.177]

Grubbs and Brunck (86) have recently reported experimental evidence supporting this mechanism. They have made an attempt to synthesize the proposed metallocyclic intermediate for the metathesis of ethene. Starting from the assumption that a mixture of WC1 and two equivalents of (C4H9)Li forms an active metathesis catalyst (49), they treated WC1 with 1,4-dilithio-2,3-dideuterobutane. One may expect that the following reaction would take place ... [Pg.149]

Grubbs and Brunck found that ethene was formed and that this product consisted of 88% C2H3D, 6% C2H4, and 6% symmetric C2H2D2. They also demonstrated that C2H4 and C2H2D2 were not formed by a secondary reaction. From this they inferred that a migration of 12% of the metal atoms had taken place. [Pg.149]

It can be concluded from the study of Grubbs and Brunck that indeed a metal-carbon cr-complex might be the key intermediate in the metathesis reaction. For the conversion of I into II several reaction pathways can be... [Pg.149]

Dlugosz J, Fraser GV, Grubb D, Keller A, Odell JA, Goggin PL (1976) Polymer 17 471... [Pg.311]


See other pages where Grubb is mentioned: [Pg.114]    [Pg.377]    [Pg.193]    [Pg.215]    [Pg.380]    [Pg.74]    [Pg.315]    [Pg.400]    [Pg.450]    [Pg.548]    [Pg.96]    [Pg.207]    [Pg.304]    [Pg.185]    [Pg.249]    [Pg.253]    [Pg.373]    [Pg.14]    [Pg.14]    [Pg.60]    [Pg.315]    [Pg.44]    [Pg.346]    [Pg.353]    [Pg.177]    [Pg.178]    [Pg.167]    [Pg.235]    [Pg.334]    [Pg.150]    [Pg.170]    [Pg.402]    [Pg.568]    [Pg.572]    [Pg.580]    [Pg.581]    [Pg.582]    [Pg.584]    [Pg.45]    [Pg.4]    [Pg.13]    [Pg.13]    [Pg.14]    [Pg.14]   
See also in sourсe #XX -- [ Pg.195 ]

See also in sourсe #XX -- [ Pg.173 ]

See also in sourсe #XX -- [ Pg.133 ]




SEARCH



Alkene metathesis Grubbs-type” complexes

Alkene metathesis Grubbs’ catalyst

Benzylidene ruthenium complex (Grubbs

Catalysts Grubb

Catalysts Grubbs catalyst

Coordination polymerization Grubbs

Domino metathesis Grubbs catalyst

Edited by Robert H. Grubbs and Anna G. Wenzel

Edited by Robert H. Grubbs and Ezat Khosravi

First generation Grubbs catalyst

Fluorous Grubbs’ catalysts

GRUBBS Olefin Metathesis

Grubb s catalyst

Grubb synthesis

Grubb, William

Grubbs

Grubbs

Grubbs Heterocycle

Grubbs Heterocyclic

Grubbs Heterogeneous

Grubbs Hexane

Grubbs Homogeneous

Grubbs Hydrocarbon

Grubbs Hydrogen

Grubbs Hydrogenated

Grubbs Hydrogenation

Grubbs Hydrophobic

Grubbs Hydrophobicity

Grubbs Hydroxyl

Grubbs Hydroxylated

Grubbs Hydroxylation

Grubbs I catalyst

Grubbs II catalyst

Grubbs III

Grubbs Test for an Outlier

Grubbs bond

Grubbs carbene

Grubbs catalysis

Grubbs catalyst chloride

Grubbs catalyst enyne metathesis

Grubbs catalysts (benzylidene carbene

Grubbs catalysts carbene reactions

Grubbs cross-metathesis

Grubbs cyclization

Grubbs diastereoselectivity

Grubbs first and second

Grubbs first and second generation catalysts

Grubbs first generation

Grubbs functionality

Grubbs group

Grubbs immobilized

Grubbs ligand substitution

Grubbs mechanism

Grubbs method

Grubbs nickel

Grubbs number

Grubbs olefin metathesis catalysts

Grubbs polyethylene

Grubbs reaction

Grubbs reaction Intermolecular

Grubbs reaction Intramolecular

Grubbs reagent / catalyst

Grubbs reagents, Tebbe methylenation

Grubbs ring-closing metathesis

Grubbs ruthenium carbene catalyst

Grubbs ruthenium catalyst

Grubbs ruthenium catalysts Subject

Grubbs s catalyst

Grubbs second generation

Grubbs second generation precatalyst

Grubbs synthesis

Grubbs test

Grubbs thermal decomposition

Grubbs third generation

Grubbs, Nobel prize

Grubbs, Robert

Grubbs, Robert H., The Olefin Metathesis Reaction

Grubbs, carbene complex

Grubbs-Catalyzed Metathesis of Eugenol with 1,4-Butenediol to Prepare a Natural Product

Grubbs-Herrmann catalyst

Grubbs-Hoveyda catalyst carbene reactions

Grubbs-Hoveyda complex

Grubbs-Hoveyda ruthenium

Grubbs-Hoveyda second-generation catalyst

Grubbs-Hoveyda-type initiators

Grubbs-Hoveyda-type precatalysts

Grubbs-Type Initiators

Grubbs-catalyzed metathesis

Grubbs-type

Grubbs-type catalysts

Grubbs-type complexes

Grubbs-type ruthenium alkylidene

Grubbs-type, Ru-based systems

Grubbs/Herrmann metathesis catalyst

Grubbs’ carbenes

Grubbs’ catalyst

Grubbs’ catalyst olefin

Grubbs’ catalyst, intramolecular

Grubbs’ catalysts advantages

Grubbs’ catalysts polynorbornenes

Grubbs’ complex

Grubbs’ initiator

Grubbs’ reagents

Grubbs’ ruthenium-carbene catalysts, transition

Grubbs’catalysts chiral

Grubbs’catalysts immobilization

Grubbs’s first-generation catalyst

Grubbs’s second-generation catalyst

Grubbs’s test

Grubbs’type methathesis

Grubb’s test

Hoveyda - Grubbs type complex

Hoveyda-Grubbs

Hoveyda-Grubbs II catalyst

Hoveyda-Grubbs catalyst

Hoveyda-Grubbs-type systems

Hoveyda-Grubbs’ second-generation

Hoyveda-Grubbs’ Catalyst

Hypothesis testing Grubbs test

Metathesis Grubbs

Metathesis Grubbs’ catalyst

Metathesis Hoveyda-Grubbs catalyst

Natural Product Synthesis using Grubbs Metathesis Lasubine II

Olefin Isomerization Promoted by the Grubbs Catalyst

ROMP with Grubbs-Type Initiators

Ring-closing metathesis reaction Hoveyda-Grubbs catalyst

Ruthenium carbene initiator (Grubb

Second generation Grubbs catalyst

Similarity ruthenium, Grubbs

Statistical tests Grubbs test

Statistics Grubbs test

The Grubbs Catalyst

The Grubbs Metathesis Reaction

The Grubbs Reaction in Organic Synthesis

© 2024 chempedia.info