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Electro-redox strategy for synthesis of dehydroaltenusin analogs through alkoxy-oxylactonizative phenol dearomatization.
- Source :
-
Tetrahedron . Feb2023, Vol. 132, pN.PAG-N.PAG. 1p. - Publication Year :
- 2023
-
Abstract
- This study reveals a strategy of electrochemical alkoxy-oxylactonization and dearomatization under metal- and external oxidant-free conditions to synthesize dehydroaltenusin analogs bearing both polycyclic cyclohexadienone and benzopyrolactone moieties. This methodology achieves phenolic radical-mediated self-dearomatization promoted by electricity at anode in an undivided cell, having good functional group tolerance, and more eco-friendliness. The obtained products are dehydroaltenusin analogs which possess potentially pharmacological activities. [Display omitted] [ABSTRACT FROM AUTHOR]
- Subjects :
- *PHENOL
*PHENOLS
*FUNCTIONAL groups
*MOIETIES (Chemistry)
*ANODES
Subjects
Details
- Language :
- English
- ISSN :
- 00404020
- Volume :
- 132
- Database :
- Academic Search Index
- Journal :
- Tetrahedron
- Publication Type :
- Academic Journal
- Accession number :
- 161552371
- Full Text :
- https://doi.org/10.1016/j.tet.2022.133238