102285-72-3

Upstream product

• 67-56-1 methanol 
• 133150-04-6 2--2-methyl-6-<<(methylamino)carbonyl>oxy>-3-oxo-3,6-dihydro-2H-pyran 
• 102285-67-6 6-hydroxy-2--2-methyl-2H-pyran-3(6H)-one 
• 74-88-4 methyl iodide 
• 102285-64-3 α-methyl-α-furfuryl alcohol 

Relevant academic research and scientific papers

Synthesis and antimicrobial properties of 2H-pyran-3(6H)-one derivatives and related compounds

The synthesis of several derivatives of 2H-pyran-3(6H)-ones and their Michael adducts is described. Phenylthio, benzenesulfonyl, p- acetylaminobenzenesulfonyl, and p-bromophenyl substituents are beneficial for activity against gram-positive bacteria. 2-[4

Products from Furans. 4. Selective Oxidation of 2-Furfuryl Alcohol Derivatives, in the Presence of Aryl Thioethers, with N-Bromosuccinimide (NBS). A New Procedure for the Preparation of 2H-Pyran-3(6H)-ones

A new general fast method (as fast as a titration) for converting 2H-furfuryl alcohols of 2H-pyran-3(6H)-ones by the use of NBS as an oxidant is presented.NBS oxidizes selectively the furfuryl alcohols without affecting thioether substituents.