Thiocarbonyl Surrogate via Combination of Potassium Sulfide and Chloroform for Dithiocarbamate Construction
Wei Tan, Niklas Jänsch, Tina Öhlmann, Franz-Josef Meyer-Almes* and Xuefeng Jiang*
*University of Applied Sciences Darmstadt, Darmstadt 64295,
Germany; East China Normal University, Shanghai 200062, P.R. China,
Email: franz-josef.meyer-almesh-da.de; xfjiang
chem.ecnu.edu.cn
W. Tan, N. Jänsch, T. Öhlmann, F.-J. Meyer-Almes, X. Jiang, Org. Lett., 2019, 21, 7484-7488.
DOI: 10.1021/acs.orglett.9b02784
see article for more reactions
Abstract
The combination of potassium sulfide and chloroform provides an efficient and practical thiocarbonyl surrogate. A variety of dithiocarbamates can be synthesized in one-pot reactions in which the thiocarbonyl motif was generated in situ.
see article for more examples
Note
Our group is directing the current research, and Prof. Meyer-Almes helped us to detect the activity of the thiocarbonyl compounds.
Xuefeng Jiang, June 1, 2020
Key Words
dithiocarbamates, multicomponent reactions
ID: J54-Y2019