Solvent-controlled regioselective arylation of indoles and mechanistic explorations. Issue 4 (13th January 2022)

• Record Type: Journal Article
• Authors: Niu, Yuan; Yan, Chao-Xian; Yang, Xin-Xin; Bai, Peng-Bo; Zhou, Pan-Pan; Yang, Shang-Dong
• Is Part Of: Organic chemistry frontiers. Volume 9:Issue 4(2022)
• Page Start: 1023
• Page End: 1032
• Publication Date: 2022-01-13
• Subjects: Chemistry, Organic -- Periodicals; 547.005
• DOI: 10.1039/d1qo01454d
• Languages: English
• ISSNs: 2052-4110

Abstract

Abstract : A new reaction for the regioselective arylation of indoles at C2 or C3 positions achieved by adjusting the solvent and with P(O) t Bu2 as an auxiliary group is reported. And the experimental results and DFT confirmed the process. Abstract : The ability to manipulate the site selectivity in C–H bond functionalization reactions is an important goal in modern chemistry. Herein, we report a new reaction strategy for the regioselective arylation of indoles at C2 or C3 positions, achieved by adjusting the solvent and with P(O) t Bu2 as an auxiliary group. The experimental results and density functional theory (DFT) calculations confirmed that Cu(iii ) dominated the formation of C3-arylation products, and the acid produced in this process initiated the migration of the C3-aryl group to the C2 site. THF, with its coordination ability, could bind acid and inhibit the migration, while the domino process in toluene proceeded smoothly. Based on this methodology, some classic indole-based fluorescent molecules synthesized by us exhibit substantially better optical properties due to the intervention of PO functional groups.