Palladium-Catalyzed One-Step Synthesis of Isoindole-1,3-diones by Carbonylative Cyclization of o -Halobenzoates and Primary Amines
✍ Scribed by Worlikar, Shilpa A.; Larock, Richard C.
- Book ID
- 126310842
- Publisher
- American Chemical Society
- Year
- 2008
- Tongue
- English
- Weight
- 199 KB
- Volume
- 73
- Category
- Article
- ISSN
- 0022-3263
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📜 SIMILAR VOLUMES
## Abstract 2‐Bromobenzaldehyde reacts with an excess of primary amines under a carbon monoxide in the presence of a catalytic amount of bis(triphenylphosphine)palladium(II) chloride together with triethylamine to give the corresponding 3‐(alkylamino)isoindolin‐1‐ones in good yields.
## Abstract A new carbon monoxide‐free, solvent‐free, single step protocol for the synthesis of isoindole‐1,3‐diones from __o__‐haloarenes using palladium acetate and xantphos catalysis is reported. The wider applicability of this protocol for several types of __o__‐iodoarenes and a few __o__‐bromo