Reductive Amination of 2,5-Furandicarbaldehyde to N,N’-Disubstituted 2,5-Bis(aminomethyl)furan under Atmospheric Pressure of Hydrogen Gas Catalyzed by a Metal–Ligand Bifunctional Iridium Catalyst

The reductive amination of 2,5-furandicarbaldehyde to N,N'-disubstituted 2,5-bis(aminomethyl)furan under atmospheric pressure of hydrogen gas has been accomplished using [Cp*Ir(2,2′-bpyO)(H2O)] as a catalyst. Functional groups in the ligand are a critical factor for the activity of the catalyst. Furthermore, the mechanistic investigation, the practical application of this system, and the reductive amination of other biobased furfuryl aldehydes were also undertaken.

Authors

Institutions

Publication Details

Journal
ACS Sustainable Chemistry & Engineering
Published
2024-12-27
DOI
https://doi.org/10.1021/acssuschemeng.4c08606
Citations
12
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
1.90

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Reductive Amination of 2,5-Furandicarbaldehyde to N,N’-Disubstituted 2,5-Bis(aminomethyl)furan under Atmospheric Pressure of Hydrogen Gas Catalyzed by a Metal–Ligand Bifunctional Iridium Catalyst

Beixuan Dong, Luyao Guo, Qixun Shi, Jinci Liang et al.
12 citations
ACS Sustainable Chemistry & Engineering
Asymmetric Hydrogenation and Catalysis
1.90
article

Reductive Amination of 2,5-Furandicarbaldehyde to N,N’-Disubstituted 2,5-Bis(aminomethyl)furan under Atmospheric Pressure of Hydrogen Gas Catalyzed by a Metal–Ligand Bifunctional Iridium Catalyst

Beixuan Dong, Luyao Guo, Qixun Shi, Jinci Liang, Feng Li, Heng You
article en
12 citations

Abstract

The reductive amination of 2,5-furandicarbaldehyde to N,N'-disubstituted 2,5-bis(aminomethyl)furan under atmospheric pressure of hydrogen gas has been accomplished using [Cp*Ir(2,2′-bpyO)(H2O)] as a catalyst. Functional groups in the ligand are a critical factor for the activity of the catalyst. Furthermore, the mechanistic investigation, the practical application of this system, and the reductive amination of other biobased furfuryl aldehydes were also undertaken.

ACS Sustainable Chemistry & EngineeringVol. 13(2)
Nanjing Tech University (CN), Dalian University of Technology (CN), Nanjing University of Science and Technology (CN), Dalian University (CN), Institute of Organic Synthesis (RU), State Key Laboratory of Fine Chemicals
National Natural Science Foundation of China
Openalex Percentile: Top 14%
Asymmetric Hydrogenation and Catalysis
1.90
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Reductive Amination of 2,5-Furandicarbaldehyde to N,N’-Disubstituted 2,5-Bis(aminomethyl)furan under Atmospheric Pressure of Hydrogen Gas Catalyzed by a Metal–Ligand Bifunctional Iridium Catalyst — Beixuan Dong, Luyao Guo, et al. · ACS Sustainable Chemistry & Engineering (2024) | TGRS Research Map | TGRS