Peer-reviewedCC BY-NC 3.0RSC Advances
Ethyl gallate as an unexplored organocatalyst: unlocking sustainable routes to isoxazolones
- 1Department of Chemistry, University of North Bengal Dist-Darjeeling West Bengal India +91-(0353)-2699001 +91-(0353)-2776381
Abstract
A simple and effective approach has been established for producing a wide range of pharmaceutically valuable functionalised 3-methyl-4-(hetero)arylmethylene isoxazole-5(4H)-ones. In this method, ethyl gallate (EG) was identified as a previously unexplored and potent organocatalyst, allowing for quick one-pot conversion to isoxazolones. The technique offers several major benefits, including metal-free conditions, good to exceptional yields, the use of readily available starting materials, and overall operational simplicity.
Related
- Unlocking the Potential of Ommatins as Sustainable Photosensitizers for Photodynamic Therapy
- Unlocking PEG-400: A Sustainable Reaction Medium for Phthalocyanine Synthesis and Pd-Catalyzed C–C Bond Formation
- Access to and unexplored reactivity of nickel-bound 5-membered O- and N-heterocyclic arynes via computational insight
- Mesoporous silica–coated gold nanorods functionalized with the D3 peptide and loaded with epigallocatechin-3-gallate reduce β-amyloid toxicity in the presence of Zn(II) ions
- Unlocking 17O Natural-Abundance Nuclear Magnetic Resonance Detection in Solids
BibTeX
@article{bhattacharjee2026ethyl,
title = {{Ethyl gallate as an unexplored organocatalyst: unlocking sustainable routes to isoxazolones}},
author = {Saptadwipa Bhattacharjee and Puja Basak and Pranab Ghosh},
journal = {RSC Advances},
year = {2026},
month = aug,
doi = {10.1039/d6ra05201k},
url = {https://doi.org/10.1039/d6ra05201k},
note = {CC BY-NC 3.0},
}
RIS
TY - JOUR
TI - Ethyl gallate as an unexplored organocatalyst: unlocking sustainable routes to isoxazolones
AU - Saptadwipa Bhattacharjee
AU - Puja Basak
AU - Pranab Ghosh
PY - 2026
DA - 2026/08/24
JO - RSC Advances
DO - 10.1039/d6ra05201k
UR - https://doi.org/10.1039/d6ra05201k
AB - A simple and effective approach has been established for producing a wide range of pharmaceutically valuable functionalised 3-methyl-4-(hetero)arylmethylene isoxazole-5(4H)-ones. In this method, ethyl gallate (EG) was identified as a previously unexplored and potent organocatalyst, allowing for quick one-pot conversion to isoxazolones. The technique offers several major benefits, including metal-free conditions, good to exceptional yields, the use of readily available starting materials, and overall operational simplicity.
SN - 2046-2069
ER -