Mechanochemical dehydrocoupling of dimethylamine borane and hydrogenation reactions using Wilkinson's catalyst

2018 ◽  
Vol 54 (60) ◽  
pp. 8355-8358 ◽  
Author(s):  
Christian Schumacher ◽  
Deborah E. Crawford ◽  
Branimir Raguž ◽  
Robert Glaum ◽  
Stuart L. James ◽  
...  

Synthesis and use of the emblematic Wilkinson's catalyst by mechanochemistry was achieved.

Author(s):  
Brian T. Heaton ◽  
Jonathan A. Iggo ◽  
Chacko Jacob ◽  
Jeyagowry Nadarajah ◽  
Marc A. Fontaine ◽  
...  

1974 ◽  
Vol 52 (17) ◽  
pp. 3000-3007 ◽  
Author(s):  
Graeme Strathdee ◽  
Russell Given

A number of polymer-attached, or anchored, catalysts of rhodium and ruthenium have been synthesized, and their activities for D2 exchange with ethanol have been measured. Among the rhodium anchored catalysts, three exhibited specific activity comparable to Wilkinson's catalyst, RhCl(PPh3)3. No polymer-attached ruthenium species had specific activities close to that of the active homogeneous catalyst RuCl2(PPh3)3. Conditions for the synthesis and optimum loading of complexing resins are discussed. Structural and kinetic comparisons are made between anchored catalysts and their homogeneous analogs.


2011 ◽  
Vol 402 (1-2) ◽  
pp. 132-138 ◽  
Author(s):  
M. Pérez-Cadenas ◽  
L.J. Lemus-Yegres ◽  
M.C. Román-Martínez ◽  
C. Salinas-Martínez de Lecea

1987 ◽  
Vol 52 (15) ◽  
pp. 3303-3307 ◽  
Author(s):  
John E. Baldwin ◽  
Timothy C. Barden ◽  
Ruth L. Pugh ◽  
Wayne C. Widdison

Synthesis ◽  
2019 ◽  
Vol 51 (18) ◽  
pp. 3529-3535 ◽  
Author(s):  
Clement Osei Akoto ◽  
Jon D. Rainier

This work outlines a suitable method for the synthesis of oxepane skeleton using iterative C-glycoside technology on the oxepene intermediate, which was synthesized utilizing Wilkinson’s catalyst [Rh(PPh3)3Cl] to generate the isomerized product in a linear synthetic manner. The central core of the oxepene motif was achieved via an olefin metathesis reaction using the Grubbs second-generation and Schrock catalysts. The synthesis of the functionalized oxepane having the desired adriatoxin E-ring relative stereochemistry was achieved starting from commercially available homopropargylic alcohol.


1985 ◽  
Vol 32 (3) ◽  
pp. 353-355 ◽  
Author(s):  
A.I. Mikaya ◽  
V.G. Zaikin ◽  
V.M. Vdovin

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