2-Bromocyclohex-1-enecarboxylic acids are carbonylatively cyclized with arylhydrazines or their hydrochlorides in tetrahydrofuran at 120 °C under carbon monoxide pressure in the presence of a catalytic amount of PdCl2 and 1,3-bis(diphenylphosphino)propane along with Et3N to give 2-anilinohydroisoindoline-1,3-diones. Copyright © 2015 John Wiley & Sons, Ltd.

Palladium-catalyzed three-component cyclization of 2-bromocyclohex-1-enecarboxylic acids with carbon monoxide and arylhydrazines leads to 2-anilinohydroisoindoline-1,3-diones

Applied Organometallic Chemistry

Palladium‐catalyzed three‐component cyclization of 2‐bromocyclohex‐1‐enecarboxylic acids with carbon monoxide and arylhydrazines leading to 2‐anilinohydroisoindoline‐1,3‐diones

Paper

Palladium‐catalyzed three‐component cyclization of 2‐bromocyclohex‐1‐enecarboxylic acids with carbon monoxide and arylhydrazines leading to 2‐anilinohydroisoindoline‐1,3‐diones

References

Citations