Skip to content
DraconiticResearch
Search Sources API
197,768 studies31 sourcesUpdated 30 min ago
Peer-reviewedCC BY-NC 3.0RSC Advances

Ethyl gallate as an unexplored organocatalyst: unlocking sustainable routes to isoxazolones

  1. 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

  1. Unlocking the Potential of Ommatins as Sustainable Photosensitizers for Photodynamic Therapy
    Arif Hussain, Anthony A. Ruberto, Harsh Bhatia +11
    Bioorganic & medicinal chemistry lettersPeer-reviewedLicence not statedFull textOrganic chemistryPMC
  2. Unlocking PEG-400: A Sustainable Reaction Medium for Phthalocyanine Synthesis and Pd-Catalyzed C–C Bond Formation
    Federica Palmeri, Venanzio Raglione, Chiara Salvitti +2
    ChemRxivPreprintCC BY-NC-NDFull textMaterials & polymersChemRxiv
  3. Access to and unexplored reactivity of nickel-bound 5-membered O- and N-heterocyclic arynes via computational insight
    Sanu Siyad Pullarat, Ali A. Younis, Gabriel N. Morais +5
    Chemical SciencePeer-reviewedCC BY-NC 3.0Full textOrganic chemistryPMC
  4. 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
    Javier Avendaño-Godoy, Carlos Álamos, Eyleen Araya +5
    Biomaterials AdvancesPeer-reviewedPublisher termsFull textNeuroscienceMaterials & polymersHAL
  5. Unlocking 17O Natural-Abundance Nuclear Magnetic Resonance Detection in Solids
    Pierre Florian, Alia Hassan, Sebastian Wegner +1
    Journal of the American Chemical SocietyPeer-reviewedPublisher termsFull textPhysical chemistryHAL
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  -