scholarly journals Hydration of nitriles using a metal–ligand cooperative ruthenium pincer catalyst

2019 ◽  
Vol 10 (45) ◽  
pp. 10647-10652 ◽  
Author(s):  
Beibei Guo ◽  
Johannes G. de Vries ◽  
Edwin Otten

The hydration of a broad range of aliphatic and (hetero)aromatic nitriles is reported via catalysis by metal–ligand cooperative Ru pincer complexes under very mild conditions.

2020 ◽  
Author(s):  
Joel D. Smith ◽  
George Durrant ◽  
Daniel Ess ◽  
Warren Piers

<div>The synthesis and characterization of an iridium polyhydride complex (Ir-H4)</div><div>supported by an electron-rich PCP framework is described. This complex readily loses molecular</div><div>hydrogen allowing for rapid room temperature hydrogen isotope exchange (HIE) at the hydridic</div><div>positions and the α-C-H site of the ligand with deuterated solvents such as benzene-d6, toluene-d8</div><div>and THF-d8. The removal of 1-2 equivalents of molecular H2 forms unsaturated iridium carbene</div><div>trihydride (Ir-H3) or monohydride (Ir-H) compounds that are able to create further unsaturation</div><div>by reversibly transferring a hydride to the ligand carbene carbon. These species are highly active</div><div>hydrogen isotope exchange (HIE) catalysts using C6D6 or D2O as deuterium sources for the</div><div>deuteration of a variety of substrates. By modifying conditions to influence the Ir-Hn speciation,</div><div>deuteration levels can range from near exhaustive to selective only for sterically accessible sites.</div><div>Preparative level deuterations of select substrates were performed allowing for procurement of</div><div>>95% deuterated compounds in excellent isolated yields; the catalyst can be regenerated by</div><div>treatment of residues with H2 and is still active for further reactions.</div>


2014 ◽  
Vol 20 (48) ◽  
pp. 15727-15731 ◽  
Author(s):  
Eran Fogler ◽  
Jai Anand Garg ◽  
Peng Hu ◽  
Gregory Leitus ◽  
Linda J. W. Shimon ◽  
...  

2014 ◽  
Vol 33 (14) ◽  
pp. 3716-3726 ◽  
Author(s):  
Aviel Anaby ◽  
Burkhard Butschke ◽  
Yehoshoa Ben-David ◽  
Linda J. W. Shimon ◽  
Gregory Leitus ◽  
...  

2015 ◽  
Vol 137 (14) ◽  
pp. 4634-4637 ◽  
Author(s):  
Moran Feller ◽  
Eyal Ben-Ari ◽  
Yael Diskin-Posner ◽  
Raanan Carmieli ◽  
Lev Weiner ◽  
...  

2003 ◽  
Vol 2003 (2) ◽  
pp. 84-86 ◽  
Author(s):  
Xiaoliang Xu ◽  
Yongmin Zhang

The intermolecular reductive coupling cyclisation of 3,3-diaryl-2-cyanoacrylonitriles or ethyl 3,3-diaryl-2-cyano-acrylates with aromatic nitriles with magnesium and catalytic iodine in THF afforded 3 H-pyrroles in good yields under neutral and mild conditions.


2009 ◽  
Vol 28 (1) ◽  
pp. 188-196 ◽  
Author(s):  
Mark C. Lipke ◽  
Robert A. Woloszynek ◽  
Liqing Ma ◽  
John D. Protasiewicz

ChemInform ◽  
2015 ◽  
Vol 46 (18) ◽  
pp. no-no
Author(s):  
Eran Fogler ◽  
Jai Anand Garg ◽  
Peng Hu ◽  
Gregory Leitus ◽  
Linda J. W. Shimon ◽  
...  

2021 ◽  
Vol 647 (14) ◽  
pp. 1397-1397
Author(s):  
Annika M. Krieger ◽  
Vivek Sinha ◽  
Adarsh V. Kalikadien ◽  
Evgeny A. Pidko

2019 ◽  
Vol 84 (7) ◽  
pp. 4072-4085 ◽  
Author(s):  
Rina Sikari ◽  
Suman Sinha ◽  
Siuli Das ◽  
Anannya Saha ◽  
Gargi Chakraborty ◽  
...  

Synlett ◽  
2020 ◽  
Vol 31 (18) ◽  
pp. 1805-1808 ◽  
Author(s):  
Zhenpeng Shen ◽  
Wenbo Liu ◽  
Xinzhe Tian ◽  
Yun-Lai Ren ◽  
Zhe Zhao

AbstractA new and effective method was developed for the synthesis of aromatic nitriles from arylacetic acids by using NaNO2 as the nitrogen source and Fe(OTf)3 as the promoter at 50 °C. A series of arylacetic acids underwent this transformation to give the targeted products in yields of 51–90%. Because of the mild conditions, the reaction is compatible with a broad range of functional groups, including ester, carboxy, hydroxy, acetamido, halo, nitro, cyano, methoxy, and even highly reactive formyl groups.


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