A Versatile Ru‐Catalyst for Selective Methylation of Diverse Organic Scaffolds Using Methanol as a C1 Synthon

Abstract Herein, we report an efficient Ru(III)‐catalyzed methylation of diverse organic scaffolds, including alcohols, ketones, nitroarenes, amines, indoles, naphthols, amides, and sulfonamides, using methanol as a green C1 synthon. A well‐defined, easy‐to‐prepare, bench‐stable Ru(III)‐catalyst featuring a redox‐active triamine ligand enables exceptional functional‐group compatibility and reactivity across multiple mechanistic pathways, including dehydrogenation, condensation, and (borrowing)‐hydrogenation. Unlike reported synthetic methodologies that require distinct catalysts for different substrate classes, our catalyst serves as a single, versatile system, eliminating the need for multiple catalysts while delivering high efficiency under mild conditions with reduced catalyst and base loading.

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Publication Details

Journal
ChemCatChem
Published
2025-11-23
DOI
https://doi.org/10.1002/cctc.202501458
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

A Versatile Ru‐Catalyst for Selective Methylation of Diverse Organic Scaffolds Using Methanol as a C1 Synthon

Santana Chakraborty, Shyamal K. Saha, Nanda Dulal Paul, Apurba Datta
ChemCatChem
Catalytic C–H Functionalization Methods
article

A Versatile Ru‐Catalyst for Selective Methylation of Diverse Organic Scaffolds Using Methanol as a C1 Synthon

Santana Chakraborty, Shyamal K. Saha, Nanda Dulal Paul, Apurba Datta
article en

Abstract

Abstract Herein, we report an efficient Ru(III)‐catalyzed methylation of diverse organic scaffolds, including alcohols, ketones, nitroarenes, amines, indoles, naphthols, amides, and sulfonamides, using methanol as a green C1 synthon. A well‐defined, easy‐to‐prepare, bench‐stable Ru(III)‐catalyst featuring a redox‐active triamine ligand enables exceptional functional‐group compatibility and reactivity across multiple mechanistic pathways, including dehydrogenation, condensation, and (borrowing)‐hydrogenation. Unlike reported synthetic methodologies that require distinct catalysts for different substrate classes, our catalyst serves as a single, versatile system, eliminating the need for multiple catalysts while delivering high efficiency under mild conditions with reduced catalyst and base loading.

ChemCatChemVol. 17(24)
Indian Institute of Engineering Science and Technology, Shibpur (IN)
Openalex Percentile: Top 73%
Catalytic C–H Functionalization Methods
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