Au/TiO2 catalyzed reductive amination of aldehydes and ketones using formic acid as reductant
Literature Information
Publication Date
2016-02-18
DOI
10.1039/C5QO00439J
Impact Factor
5.281
Authors
Shengzong Liang, Paige Monsen, Gerald B. Hammond, Bo Xu
View Original
Abstract
The combination of commercial easily available Au/TiO2 as catalyst and cost-effective formic acid as reductant was able to render reductive amination of various carbonyl compounds. Aldehydes and ketones were converted into secondary and tertiary amines in good to excellent yields. The supported gold nanoparticles could be easily recycled by simple filtration.
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Source Journal
Organic Chemistry Frontiers
CiteScore:
7.8
Self-citation Rate:
8.7%
Articles per Year:
724
Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry
Recommended Compounds
![2-{3-[4-(3-Chlorophenyl)-1-piperazinyl]propyl}[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one hydrochloride (1:1) structure](https://static.chemtradehub.com/structs/253/25332-39-2-496e.webp "2-{3-[4-(3-Chlorophenyl)-1-piperazinyl]propyl}[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one hydrochloride (1:1) structure")
2-{3-[4-(3-Chlorophenyl)-1-piperazinyl]propyl}[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one hydrochloride (1:1)
CAS Number:
25332-39-2
Molecular Formula:
C19H23Cl2N5O
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