Efficient transfer hydrogenation of carbonyl compounds catalyzed by selenophenolato hydrido iron(II) complexes

2019 ◽  
Vol 124 ◽  
pp. 32-35 ◽  
Author(s):  
Yangyang Wang ◽  
Zhengyin Du ◽  
Tingting Zheng ◽  
Hongjian Sun ◽  
Xiaoyan Li
2020 ◽  
Vol 49 (2) ◽  
pp. 453-465 ◽  
Author(s):  
Rosario Figliolia ◽  
Paolo Cavigli ◽  
Clara Comuzzi ◽  
Alessandro Del Zotto ◽  
Denise Lovison ◽  
...  

Robust and easily accessible CNNOMe pincer ruthenium complexes show unprecedented selectivity and productivity in the TH of lignocellulose-derived carbonyl compounds with 2-propanol.


2019 ◽  
Vol 7 (9) ◽  
pp. 8893-8899 ◽  
Author(s):  
Sudakar Padmanaban ◽  
Gunniya Hariyanandam Gunasekar ◽  
Mearae Lee ◽  
Sungho Yoon

Catalysts ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 1338
Author(s):  
Marek Gliński ◽  
Ewa M. Iwanek (nee Wilczkowska) ◽  
Urszula Ulkowska ◽  
Agnieszka Czajka ◽  
Zbigniew Kaszkur

The first aim of the research was to synthesize a pure Upsalite, which is an amorphous form of MgCO3, by modifying a procedure described in the literature, so that it would be the precursor of a high-surface, amorphous magnesium oxide. The results indicate that within the studied reaction conditions, the type of alcohol used as the reactant has the most pronounced effect on the yield of reaction. From the two alcohols that led to the highest yield of Upsalite, methanol gave a substantially larger surface area (794 vs. 191 m2 g−1). The optimized synthesis conditions of Upsalite were used to obtain MgO via thermolysis, whose activity in the transfer hydrogenation reaction (THR) from ethanol, 2-propanol and 2-pentanol to various carbonyl compounds was determined. The optimal conditions for the thermolysis were as follows: vacuum, T = 673 K as the final temperature, and a heating rate of 2 deg min−1. The high-surface, amorphous magnesia (SBET = 488 m2 g−1) was found to be a very selective catalyst to 4-t-butylcyclohexanone in THR, which led to a diastereoselectivity of over 94% to the E-isomer of 4-t-butylcyclohexanol for more than 3 h, with conversions of up to 97% with either 2-propanol or 2-pentanol as the hydrogen donor. In the case of acrolein and 2-n-propylacrolein being used as the hydrogen acceptors, the unsaturated alcohol (UOL) was the main product of the reaction, with higher UOL yields noted for ethanol than 2-propanol.


2020 ◽  
Vol 44 (20) ◽  
pp. 8223-8231 ◽  
Author(s):  
Punitharaj Vasanthakumar ◽  
Dharmalingam Sindhuja ◽  
Duraisamy Senthil Raja ◽  
Chia-Her Lin ◽  
Ramasamy Karvembu

Fe and Cr based MOFs (MIL-88B) act as efficient and reusable catalysts for transfer hydrogenation of carbonyl compounds including bio-derived substrates.


Catalysts ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 162 ◽  
Author(s):  
Alberto Mannu ◽  
Arnald Grabulosa ◽  
Salvatore Baldino

The reduction of ketones through homogeneous transfer hydrogenation catalyzed by transition metals is one of the most important routes for obtaining alcohols from carbonyl compounds. The interest of this method increases when opportune catalytic precursors are able to perform the transformation in an asymmetric fashion, generating enantiomerically enriched chiral alcohols. This reaction has been extensively studied in terms of catalysts and variety of substrates. A large amount of information about the possible mechanisms is available nowadays, which has been of high importance for the development of systems with excellent outcomes in terms of conversion, enantioselectivity and Turn Over Frequency. On the other side, many mechanistic aspects are still unclear, especially for those catalytic precursors which have shown only moderate performances in transfer hydeogenation. This is the case of neutral [RuCl2(η6-arene)(P)] and cationic [Rh(PP)2]X (X = anion; P and PP = mono- and bidentate phosphine, respectively) complexes. Herein, a summary of the known information about the Transfer Hydrogenation catalyzed by these complexes is provided with a continuous focus on the more relevant mechanistic features.


2020 ◽  
Vol 49 (16) ◽  
pp. 5024-5028 ◽  
Author(s):  
Vasudeva Rao Bakuru ◽  
Debabrata Samanta ◽  
Tapas Kumar Maji ◽  
Suresh Babu Kalidindi

Ammonia borane with both hydridic and protic hydrogens in its structure acted as an efficient transfer hydrogenation agent for selective transformation of alkynes into alkenes in non-protic solvents.


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