A rapid access to aliphatic sulfonyl fluorides
Sulfonyl fluorides are important probes in chemical biology and molecular pharmacology. Here, the authors report a mild visible light-mediated decarboxylative fluorosulfonylethylation for the synthesis of aliphatic sulfonyl fluorides from a wide range of carboxylic acids, including natural products...
Main Authors: | Ruting Xu, Tianxiao Xu, Mingcheng Yang, Tianpeng Cao, Saihu Liao |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Publishing Group
2019-08-01
|
Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-019-11805-6 |
Similar Items
-
Rh-Catalyzed Highly Enantioselective Synthesis of Aliphatic Sulfonyl Fluorides
by: Balakrishna Moku, et al.
Published: (2019-11-01) -
Decarboxylative thiolation of redox-active esters to free thiols and further diversification
by: Tianpeng Cao, et al.
Published: (2020-10-01) -
Tuning the sulfonyl fluoride warhead towards new proteasome inhibitors : alpha-substituted sulfonyl fluorides and vinyl sulfonyl fluorides
by: Herrero Alvarez, Natalia
Published: (2017) -
Reactivities of aliphatic fluorides /
by: Beck, Leonard Henry
Published: (1959) -
Development of Arene Sulfonyl Fluoride-based Probes for Proteomic Applications
by: Yu-Ling Hsu, et al.
Published: (2008)