Efficient introduction of perfluorinated tails onto aromatic rings has been achieved by Heck reaction between perfluoroalkenes and arenediazonium salts, catalysed by palladium acetate. Subsequent transition metal catalysed hydrogenation of the double bond afforded a large variety of aromatic compoun
Access to Paullone Analogues by Intramolecular Heck Reaction
✍ Scribed by Lionel Joucla; Florence Popowycz; Olivier Lozach; Laurent Meijer; Benoît Joseph
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- German
- Weight
- 140 KB
- Volume
- 90
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The syntheses of paullone (1a) and three paullone derivatives, including a sulfur analogue (2a), a tricyclic derivative (2b), and a ring‐enlarged variant (2c), are described, Pd‐catalyzed intramolecular Heck reaction being the key step. The kinase‐inhibitory properties of the novel paullone analogues were investigated.
📜 SIMILAR VOLUMES
## Abstract A novel access to α‐methylene‐γ‐sultams __via__ the intramolecular Heck reaction of α‐bromovinylsulfonamides derived from allylic amines is reported. These heterocycles are potent Michael acceptors towards sulfur nucleophiles.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract For Abstract see ChemInform Abstract in Full Text.