Transition-metal-free formal cross-coupling of aryl methyl sulfoxides and alcohols via nucleophilic activation of C-S bond
Cross-coupling processes without the use of transition metals are challenging to achieve. Here, the authors show a transition-metal-free cross-coupling utilizing aryl(heteroaryl) methyl sulfoxides and alcohols to afford alkyl aryl(heteroaryl) ethers and propose a nucleophilic addition mechanism base...
Saved in:
Main Authors: | Guolin Li, Yexenia Nieves-Quinones, Hui Zhang, Qingjin Liang, Shuaisong Su, Qingchao Liu, Marisa C. Kozlowski, Tiezheng Jia |
---|---|
Format: | article |
Language: | EN |
Published: |
Nature Portfolio
2020
|
Subjects: | |
Online Access: | https://doaj.org/article/1679d5adbdd047cb86a6aaee0fff8c7d |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Nucleophilic arylation with tetraarylphosphonium salts
by: Zuyong Deng, et al.
Published: (2016) -
Formal group insertion into aryl C‒N bonds through an aromaticity destruction-reconstruction process
by: Dandan Han, et al.
Published: (2018) -
Stereoselective oxidative glycosylation of anomeric nucleophiles with alcohols and carboxylic acids
by: Tianyi Yang, et al.
Published: (2018) -
Autocatalytic photoredox Chan-Lam coupling of free diaryl sulfoximines with arylboronic acids
by: Cong Wang, et al.
Published: (2021) -
Thioketone-directed rhodium(I) catalyzed enantioselective C-H bond arylation of ferrocenes
by: Zhong-Jian Cai, et al.
Published: (2019)