New Insight into the Reactivity of Pyridine-Functionalized Phosphine Complexes of Ruthenium(II) with Respect to Olefin Metathesis and Transfer Hydrogenation

2008 ◽  
Vol 27 (6) ◽  
pp. 1193-1206 ◽  
Author(s):  
Emmanuelle Mothes ◽  
Stephane Sentets ◽  
Maria Asuncion Luquin ◽  
René Mathieu ◽  
Noël Lugan ◽  
...  
Author(s):  
David M. Kaphan ◽  
Kelsey R. Brereton ◽  
Rachel C. Klet ◽  
Ryan J. Witzke ◽  
Alexander J. M. Miller ◽  
...  

2020 ◽  
Vol 10 (1) ◽  
pp. 169-179 ◽  
Author(s):  
Li Zhou ◽  
Datai Liu ◽  
Haiyi Lan ◽  
Xiujian Wang ◽  
Cunyuan Zhao ◽  
...  

The origin of different catalytic activity between two structurally similar Lewis basic bifunctional catalysts.


2019 ◽  
Vol 220 ◽  
pp. 45-57 ◽  
Author(s):  
Daniel B. G. Berry ◽  
Anna Codina ◽  
Ian Clegg ◽  
Catherine L. Lyall ◽  
John P. Lowe ◽  
...  

Operando spectroscopy shows a transition from dehydrogenation to hydrogen transfer during the reaction, and allows measuring optimal conditions for maximum rate and efficiency.


ChemInform ◽  
2015 ◽  
Vol 46 (26) ◽  
pp. no-no
Author(s):  
Grzegorz Krzysztof Zielinski ◽  
Cezary Samojlowicz ◽  
Tomasz Wdowik ◽  
Karol Grela

2015 ◽  
Vol 13 (9) ◽  
pp. 2684-2688 ◽  
Author(s):  
Grzegorz Krzysztof Zieliński ◽  
Cezary Samojłowicz ◽  
Tomasz Wdowik ◽  
Karol Grela

A remarkably selective system for transfer hydrogenation of alkenes, composed of Grubbs’ ruthenium metathesis catalyst and HCOONa/HCOOH, is presented. This system can also be formed directly after a metathesis reaction to effect hydrogenation in a single-pot.


2006 ◽  
Vol 691 (24-25) ◽  
pp. 5312-5325 ◽  
Author(s):  
Werner Janse van Rensburg ◽  
Petrus J. Steynberg ◽  
Megan M. Kirk ◽  
Wolfgang H. Meyer ◽  
Grant S. Forman

2019 ◽  
Vol 48 (14) ◽  
pp. 4625-4635 ◽  
Author(s):  
Daniela A. Hey ◽  
Pauline J. Fischer ◽  
Walter Baratta ◽  
Fritz E. Kühn

The versatile precursor Ru(O2CCF3)2(PPh3)2 was isolated and used for the synthesis of ruthenium(ii) trifluoroacetate complexes, active in ketone transfer hydrogenation.


2019 ◽  
Author(s):  
Alexandre Djurovic ◽  
Marie Vayer ◽  
Zhilong Li ◽  
Régis Guillot ◽  
Jean Pierre Baltaze ◽  
...  

We report a catalytic tandem process involving a ring-closing carbonyl-olefin metathesis and a transfer hydrogenation. 1,4-Cyclohexadiene has been used as H<sub>2 </sub>surrogate to reduce the cyclic alkenes formed after the metathesis step. The same NHC-stabilized cationic gallium(III) complex, [IPr<b><sub>˙</sub></b>GaCl<sub>2</sub>][SbF<sub>6</sub>], performs the two steps with functional group tolerance. This reaction is stereoselective, leading either to 1,2-<i>cis</i>disubstituted cyclopentanes or to a variety of cyclohexanes. DFT computations support an unexpected mechanism involving the activation of 1,4-cyclohexadiene by superelectrophilic gallium(III) dimers.


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