Ligand-Enabled C-H Olefination and Lactonization of Benzoic Acids and Phenylacetic Acids via Palladium Catalyst.

Org Lett

Engineering Research Centre of Pharmaceutical Process Chemistry, Ministry of Education, School of Pharmacy, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, P. R. China.

Published: January 2022

A novel ligand propan-2-one -(-tolylcarbamoyl) oxime () has been developed to promote C(sp)-H olefination of benzoic acids and phenylacetic acids via a palladium catalyst. With the subsequent lactonization of the olefinated products through 1,4-addition, highly monoselective cyclic lactone products of benzofuranones and benzopyrones were obtained in moderate to excellent yields. The DFT calculation demonstrated that the novel ligand propan-2-one -(-tolylcarbamoyl) oxime () could improve the C-H activation reaction to give cyclic lactone products elegantly.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.orglett.1c04000DOI Listing

Publication Analysis

Top Keywords

benzoic acids
8
acids phenylacetic
8
phenylacetic acids
8
acids palladium
8
palladium catalyst
8
novel ligand
8
ligand propan-2-one
8
propan-2-one --tolylcarbamoyl
8
--tolylcarbamoyl oxime
8
cyclic lactone
8

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!