Utilization of Cooperative Ni Catalyst for Selective Transfer Hydrogenation of N-Heteroarenes with Minimal Hydrogen Surrogate

Herein, an air-stable cooperative Ni(II)-NNN catalyst (<b>1</b>) bearing a bis(2-hydroxy pyridine) ligand was synthesized for the selective transfer hydrogenation of quinoline derivatives to 1,2,3,4-tetrahydro derivatives utilizing minimal loading of Me<sub>2</sub>NHBH<sub>3</sub> as a hydrogen surrogate via a borylated product intermediate. Mechanistic studies include the identification of catalytically relevant deprotonated intermediate <b>1a</b>, which sheds light on the hydride and proton transfer to the quinoline derivatives via the participation of the functionalized protic ligand arm.

Authors

Institutions

Publication Details

Journal
Inorganic Chemistry
Published
2026-01-16
DOI
https://doi.org/10.1021/acs.inorgchem.5c05034
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Utilization of Cooperative Ni Catalyst for Selective Transfer Hydrogenation of N-Heteroarenes with Minimal Hydrogen Surrogate

Prosenjit Daw, Satabdee Tanaya Sahoo, Gowtham Kenguva, Rambabu Dandela et al.
Inorganic Chemistry
Asymmetric Hydrogenation and Catalysis
article

Utilization of Cooperative Ni Catalyst for Selective Transfer Hydrogenation of N-Heteroarenes with Minimal Hydrogen Surrogate

Prosenjit Daw, Satabdee Tanaya Sahoo, Gowtham Kenguva, Rambabu Dandela, Bijan Mondal
article en

Abstract

Herein, an air-stable cooperative Ni(II)-NNN catalyst (<b>1</b>) bearing a bis(2-hydroxy pyridine) ligand was synthesized for the selective transfer hydrogenation of quinoline derivatives to 1,2,3,4-tetrahydro derivatives utilizing minimal loading of Me<sub>2</sub>NHBH<sub>3</sub> as a hydrogen surrogate via a borylated product intermediate. Mechanistic studies include the identification of catalytically relevant deprotonated intermediate <b>1a</b>, which sheds light on the hydride and proton transfer to the quinoline derivatives via the participation of the functionalized protic ligand arm.

Inorganic Chemistry
Indian Institute of Science Education and Research Berhampur (IN), Oil India (India) (IN)
Openalex Percentile: Top 87%
Asymmetric Hydrogenation and Catalysis
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.