A photoredox/nickel dual-catalytic strategy for benzylic C–H alkoxylation. Issue 24 (1st November 2021)

• Record Type: Journal Article
• Authors: Dong, Min; Jia, Yuqi; Zhou, Wei; Gao, Jinlai; Lv, Xiaoqing; Luo, Fan; Zhang, Yongqiang; Liu, Shihui
• Is Part Of: Organic chemistry frontiers. Volume 8:Issue 24(2021)
• Page Start: 6881
• Page End: 6887
• Publication Date: 2021-11-01
• Subjects: Chemistry, Organic -- Periodicals; 547.005
• DOI: 10.1039/d1qo01421h
• Languages: English
• ISSNs: 2052-4110

Abstract

Abstract : Reported herein is a photoredox/nickel dual-catalyzed benzylic C–H alkoxylation and the protocol features broad substrate scope and excellent functional group compatibility. Abstract : Benzylic C–H alkoxylation via C–H/O–H cross-coupling represents an attractive strategy to access highly functionalized benzylic ethers but remains challenging due to the difficulty in improving the efficiency and selectivity. Herein we wish to report a highly efficient photoredox/nickel dual-catalytic strategy for the site-selective and chemoselective benzylic C–H alkoxylation using readily available Selectfluor as the oxidant. The protocol features broad substrate scope and excellent functional group compatibility and allows the transformation of various of alcohols to pharmaceutically relevant benzylic ethers in moderate to excellent yields under mild reaction conditions. CD3 OD was well tolerated, providing a useful synthetic tool for the synthesis of valuable deuterated pharmaceutical molecules. This method is also highlighted by the late-stage introduction of valuable alkoxy groups into pharmaceutical molecules and the structure modification of saccharides.