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Arylation of Benzo-Fused 1,4-Quinones by the Addition of Boronic Acids under Dicationic Pd(II)-Catalysis
- Source :
- Digital.CSIC. Repositorio Institucional del CSIC, instname
- Publication Year :
- 2009
- Publisher :
- American Chemical Society (ACS), 2009.
-
Abstract
- The first examples of the direct arylation of benzo-fused 1,4-quinones by the dicationic Pd(II)-catalyzed addition of arylboronic acids are reported. The addition reaction is carried out under very mild conditions (dioxane-H2O, rt, open air atmosphere) and is tolerant of free OH groups. In addition, the reaction shows high regioselectivity when using nonsymmetrical quinones as starting materials.<br />Projects UCM-BSCH GR58/08-910815 and CTQ2006-15279-C03-01 (both to A.G.C.), and SAF2006- 04698 (to M.T.M.), are gratefully acknowledged for financial support.
- Subjects :
- Juglone
Anthraquinones
Biochemistry
Catalysis
chemistry.chemical_compound
Organic chemistry
Physical and Theoretical Chemistry
Open air
Natural products
Addition reaction
Molecular Structure
Organic Chemistry
Quinones
Regioselectivity
Stereoisomerism
Arylation
Boronic Acids
Palladium catalysis
Arylboronic acids
Ligand effects
chemistry
Palladium
Naphthoquinones
Subjects
Details
- ISSN :
- 15237052 and 15237060
- Volume :
- 11
- Database :
- OpenAIRE
- Journal :
- Organic Letters
- Accession number :
- edsair.doi.dedup.....c23c9bfc13381e9c81863ed3560f723c