Deoxygenation of carbonyl compounds using an alcohol as an efficient reducing agent catalyzed by oxo-rhenium complexes

2016 ◽  
Vol 18 (9) ◽  
pp. 2675-2681 ◽  
Author(s):  
Joana R. Bernardo ◽  
Ana C. Fernandes

The catalytic system 3-pentanol/ReOCl3(SMe2)(OPPh3) was very efficient for the deoxygenation of carbonyl compounds.

2002 ◽  
Vol 80 (7) ◽  
pp. 779-788 ◽  
Author(s):  
Giancarlo Verardo ◽  
Paola Geatti ◽  
Elena Pol ◽  
Angelo G Giumanini

α-Amino acids and α-amino methyl esters are easily converted to their N-monoalkyl derivatives by a reductive condensation reaction using several carbonyl compounds in the presence of sodium borohydride. This reducing agent has shown a wide versatility with minor but essential procedural variations. The reaction allows the α-monodeuterium labeling of the new N-substituent by use of sodium borodeuteride.Key words: α-amino acid, α-amino methyl esters, sodium borohydride, reductive N-monoalkylation, carbonyl compounds.


2019 ◽  
Vol 21 (3) ◽  
pp. 614-626 ◽  
Author(s):  
Francesco Ferlin ◽  
Matteo Cappelletti ◽  
Riccardo Vivani ◽  
Monica Pica ◽  
Oriana Piermatti ◽  
...  

Zirconium phosphate bearing aminoethyl groups on the layer surface, ZP(AEP), was used to immobilize AuNPs. The gold-based catalyst proved its high efficiency for the chemoselective reduction of nitroarenes under both batch and flow conditions by using NaBH4 as a reducing agent.


Synthesis ◽  
1984 ◽  
Vol 1984 (04) ◽  
pp. 308-310 ◽  
Author(s):  
Hidenori Chikashita ◽  
Makoto Miyazaki ◽  
Kazuyoshi Itoh

2015 ◽  
Vol 69 ◽  
pp. 228-233 ◽  
Author(s):  
Mattia Bartoli ◽  
Luca Rosi ◽  
Giorgio Petrucci ◽  
Lidia Armelao ◽  
Werner Oberhauser ◽  
...  

Synlett ◽  
2021 ◽  
Author(s):  
Margarita Escudero-Casao ◽  
Giulia Licini ◽  
Manuel Orlandi

The transition metal catalyzed α-arylation of carbonyl compounds was first reported by Buchwald and Hartwig in 1997. This transformation has been used and studied extensively over the last two decades. Enantioselective variants were also developed that allow for controlling the product stereochemistry. However, these suffer several limitations in the context of formation of tertiary stereocenters. Presented here is our group’s contribution to this research area. The chiral Cu-bis(phosphine) dioxides catalytic system that we reported allowed accessing the enantioselective α-arylation of ketones that were not suitable for this transformation before in good yields and er up to 97.5:2.5. Preliminary insight and speculation concerning the reaction mechanism involving the unusual pairing of bis(phosphine) dioxides with transition metal catalysts is also given.


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