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A metal-free strategy for the cross-dehydrogenative coupling of 1,3-dicarbonyl compounds with 2-methoxyethanol.
- Source :
-
Organic & biomolecular chemistry [Org Biomol Chem] 2022 Feb 09; Vol. 20 (6), pp. 1226-1230. Date of Electronic Publication: 2022 Feb 09. - Publication Year :
- 2022
-
Abstract
- Here, we report a metal-free approach for the construction of methylene-bridged bis-1,3-dicarbonyl compounds via cross-dehydrogenative coupling of 1,3-dicarbonyl compounds with 2-methoxyethanol. In addition, we have extended this methodology to synthesize tetra-substituted pyridine derivatives using 1,3-dicarbonyl, 2-methoxyethanol and NH <subscript>4</subscript> OAc in one step. The key advantages include accepting a wide range of substrates, utilizing O <subscript>2</subscript> as the sole oxidant, and synthesizing biologically active compounds such as 1,4-dihydropyridine and pyrazole.
Details
- Language :
- English
- ISSN :
- 1477-0539
- Volume :
- 20
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Organic & biomolecular chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 35040852
- Full Text :
- https://doi.org/10.1039/d1ob02290c