Light-driven synthesis of 3-(hetero)aryl/alkyl-1-indanone derivatives from indan-1,3-diones and boronic acids via N-tosylhydrazones
<h2>Abstract</h2> An efficient methodology has been developed for synthesizing 3-(hetero)aryl/alkyl-indan-1-ones, which are highly valued scaffolds in chemistry. This method allows the mono(hetero)arylation/alkylation of indane-1,3-diones with (hetero)aryl/alkyl boronic acids under light-induced reaction conditions with the aid of K<sub>3</sub>PO<sub>4</sub>. A three-component approach also achieved the one-pot synthesis of 3-aryl/alkyl-indan-1-ones in good yields. UV absorption studies observed light-induced cleavage of the N–S bond of <i>N</i>-tosylhydrazone. We have also demonstrated the synthetic utility of C<sub>3</sub>-substituted aryl/alkyl-indan-1-ones and synthesized a biologically active molecule.
Authors
- Dongari Yadagiri (ORCID: https://orcid.org/0000-0001-8305-3519)
- Pokhriyal Yamini (ORCID: https://orcid.org/0000-0002-2097-7359)
- Mohammad Junaid (ORCID: https://orcid.org/0009-0002-3777-3667)
Institutions
- Indian Institute of Technology Roorkee (IN)
Publication Details
- Journal
- Tetrahedron Chem
- Published
- 2025-12-01
- DOI
- https://doi.org/10.1016/j.tchem.2025.100150
- Citations
- 1
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.94