Cross‐Dehydrogenative Coupling Reaction of 4‐Aminophenols with 2‐Naphthols Catalyzed by a Mesoporous Silica‐Supported Oxovanadium Catalyst

Abstract Cross‐dehydrogenative coupling (CDC) reactions offer an atom‐economical approach for synthesizing biaryl compounds by directly forming C─C bonds from the C─H bonds of two aromatic molecules. In this study, the CDC reaction between 4‐aminophenols and 2‐naphthols was successfully catalyzed using a mesoporous silica‐supported oxovanadium catalyst. This reaction involved the catalytic, chemo‐ and regio‐selective oxidation of 4‐aminophenols, with molecular oxygen as the terminal oxidant, eliminating the need for stoichiometric chemical oxidants, thereby making the reaction more environmentally friendly.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2025-09-17
DOI
https://doi.org/10.1002/ajoc.202500537
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Cross‐Dehydrogenative Coupling Reaction of 4‐Aminophenols with 2‐Naphthols Catalyzed by a Mesoporous Silica‐Supported Oxovanadium Catalyst

Tomoya Nishio, Kwihwan Kobayashi, Yutaro Ito, Kyohei Kanomata et al.
Asian Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
article

Cross‐Dehydrogenative Coupling Reaction of 4‐Aminophenols with 2‐Naphthols Catalyzed by a Mesoporous Silica‐Supported Oxovanadium Catalyst

Tomoya Nishio, Kwihwan Kobayashi, Yutaro Ito, Kyohei Kanomata, Shuji Akai, Koichiro Masuda, Kengo Kasama, Hiroshi Aoyama, Atsushi Kimishima, Jihoon Moon, Yasushi Kanzaki
article en

Abstract

Abstract Cross‐dehydrogenative coupling (CDC) reactions offer an atom‐economical approach for synthesizing biaryl compounds by directly forming C─C bonds from the C─H bonds of two aromatic molecules. In this study, the CDC reaction between 4‐aminophenols and 2‐naphthols was successfully catalyzed using a mesoporous silica‐supported oxovanadium catalyst. This reaction involved the catalytic, chemo‐ and regio‐selective oxidation of 4‐aminophenols, with molecular oxygen as the terminal oxidant, eliminating the need for stoichiometric chemical oxidants, thereby making the reaction more environmentally friendly.

Asian Journal of Organic ChemistryVol. 14(11)
Juntendo University Urayasu Hospital (JP), Midorigaoka Hospital (JP), University of Toyama (JP), National Institute of Advanced Industrial Science and Technology (JP), The University of Osaka (JP)
Japan Agency for Medical Research and Development, National Institute of Advanced Industrial Science and Technology, Tokuyama Science Foundation, Amano Institute of Technology, Sekisui Chemical, Japan Society for the Promotion of Science
Openalex Percentile: Top 81%
Catalytic C–H Functionalization Methods
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Cross‐Dehydrogenative Coupling Reaction of 4‐Aminophenols with 2‐Naphthols Catalyzed by a Mesoporous Silica‐Supported Oxovanadium Catalyst — Tomoya Nishio, Kwihwan Kobayashi, et al. · Asian Journal of Organic Chemistry (2025) | TGRS Research Map | TGRS