Facile Synthesis of 1,3-Diaryl-propanones Through Heck Reaction
- 1 June 1998
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 28 (12) , 2311-2316
- https://doi.org/10.1080/00397919808007049
Abstract
1,3-diaryl propanones (1a-6a) and 1,3-diaryl-2-carbomethoxy-propanones (1b-6b) have been synthesized through facile palladium catalysed arylation of Baylis- Hillman adducts.Keywords
This publication has 10 references indexed in Scilit:
- On the efficiency of tetraalkylammonium salts in Heck type reactionsTetrahedron, 1996
- The Baylis-Hillman reaction: A novel carbon-carbon bond forming reactionTetrahedron, 1996
- Effects of High Pressure on the Heck Reaction. Is It Possible to Control Dehydropalladation of Alkylpalladium Intermediates Having β-Hydrogens?Tetrahedron Letters, 1995
- Formation of CC bond in solid phase synthesis using the heck reactionTetrahedron Letters, 1995
- Aqueous Heck reaction of amino acid derived arenediazonium salts: Semisynthetic modification of phenylalanine and tyrosineTetrahedron Letters, 1995
- Microwave Mediated Extensive Rate Enhancement of the Baylis-Hillman ReactionSynlett, 1994
- Palladium catalysed phenylation of allylic alcohols; dramatic effect of tertiary amines on the reaction rateJournal of the Chemical Society, Chemical Communications, 1988
- Diarylpropanes from the wood of Iryanthera grandisPhytochemistry, 1986
- Palladium‐Catalyzed Vinylation of Organic HalidesPublished by Wiley ,1982
- Additional flavanoids in Gliricidia sepiumPhytochemistry, 1979