One-pot synthesis of tetrahydrofuran derivatives via a divalent palladium-catalyzed three-component coupling
β Scribed by Guosheng Liu; Xiyan Lu
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 326 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Under divalent palladium catalysis, a three-component coupling reaction for synthesizing tetrahydrofuran derivatives has been established. The reaction involves the intramolecular carbopalladation of an alkyne with a carbanion which was generated from the addition of an alkoxide ion to an alkene derivative, followed by allylic chloride insertion to the C Pd bond and quenching the C Pd bond by b-heteroatom elimination in the presence of excess chloride ions.
π SIMILAR VOLUMES
The synthesis of various polyhydroquinoline derivatives has been achieved using catalytic amounts of green, inexpensive and eco-friendly Keggin type heteropolyacid. The products were obtained in high yields.
## Abstract magnified image Oxazino[5,6β__f__]quinolinβ3βone derivatives have been synthesized in a oneβpot, and efficient process by condensation of 6βquinolinol, aromatic aldehydes and urea under microwaveβassisted and thermal solventβfree conditions.