Electrosynthesis using a fluoride ion mediator. Part V: Fluoride ion mediated anodic methoxylation and acetoxylation of thiazolidines, 1,3-oxathiolanes, and 1,3-dithiolanes-Science-Chemical Encyclopedia-lookchem

Electrosynthesis using a fluoride ion mediator. Part V: Fluoride ion mediated anodic methoxylation and acetoxylation of thiazolidines, 1,3-oxathiolanes, and 1,3-dithiolanes
Add time:07/11/2019 Source:sciencedirect.com

Anodic methoxylation and acetoxylation reactions of five membered cyclic sulfides such as thiazolidines, 1,3-oxathiolanes and 1,3-dithiolanes, which have been reported to not always undergo the Pummerer reaction, were successfully carried out by using a fluoride ion mediator.

We also recommend Trading Suppliers and Manufacturers of 2,2-Diisopropyl-1,3-oxathiolane (cas 16047-99-7). Pls Click Website Link as below: cas 16047-99-7 suppliers

Prev:Synthesis and application of ionic liquid functionalized β-cyclodextrin, mono-6-deoxy-6-(4-amino-1,2,4-triazolium)-β-cyclodextrin chloride, as chiral selector in capillary electrophoresis
Next: N-Sulfonyl acetylketenimine as a highly reactive intermediate for synthesis of N-Aroylsulfonamides)

Click to view details

Encyclopedia