Microwave-Accelerated Solvent-Free Synthesis of Thioketones, Thiolactones, Thioamides, Thionoesters, and Thioflavonoids
Rajender S. Varma* and Dalip Kumar
*Sustainable Technology Division, National Risk Management Research
Laboratory, U.S. Environmental Protection Agency, 26 West Martin Luther King
Drive, MS 443, Cincinnati, Ohio 45268, Email: varma.rajender
epa.gov
R. S. Varma, D. Kumar, Org. Lett., 1999, 1, 697-700.
DOI: 10.1021/ol990629a
Abstract
An expeditious, solvent-free, and high yield conversion of ketones, flavones, isoflavones, lactones, amides, and esters to the corresponding thio analogues is described utilizing Lawesson's reagent in a process that circumvents the use of dry solvents and excess of the reagent.
see article for more examples
While ads financed 62% of the published abstracts in 2024, donations allowed us to publish additional 12%. 26% of the abstracts have been published voluntarly. If you kindly donate, we can publish more freely accessible information and help the chemical community even more:
If you don't like pawalls or a flood of more and more advertising, then you can send a clear signal here!
Key Words
Lawesson's Reagent, Thioketones, Thioamides, Thionoesters Microwave Synthesis
ID: J54-Y1999-400
