Journal of Organic Chemistry p. 10643 - 10650 (2015)
Update date:2022-09-26
Topics:
Zhang, Ying
Chen, Jing-Lei
Chen, Zhen-Bang
Zhu, Yong-Ming
Ji, Shun-Jun
An efficient synthesis of 2-substituted indene-1,3(2H)-diones from stable and readily available 1-(2-halophenyl)-1,3-diones by employing phenyl formate as a CO source has been developed. The reaction occurred via palladium-catalyzed intramolecular carbonylative annulation using K3PO4 as a base and DMSO as a solvent at 95 °C. In this protocol, the reaction showed a broad substrate scope with good to excellent yields.
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