102285-69-8

Upstream product

• 65085-83-8 4'-(phenylsulfonyl)acetophenone 
• 102285-64-3 α-methyl-α-furfuryl alcohol 
• 81830-82-2 α-methyl-α-furfuryl alcohol 

Downstream Products

• 102285-73-4 2--2-methyl-2H-pyran-3,5-dione 
• 81830-88-8 2--2-methyl-6-<<(methylamino)carbonyl>oxy>-3-oxo-3,6-dihydro-2H-pyran 
• 81830-87-7 5-<4-(benzenesulfonyl)phenyl>-1,5-dimethyldihydro-<1H,7H>-5H-pyrano<3,2-d>oxazole-2,6-dione 
• 81830-87-7 5-(4-Benzenesulfonyl-phenyl)-1,5-dimethyl-dihydro-pyrano[3,2-d]oxazole-2,6-dione 
• 145371-50-2 2--2-methyl-6-<<(ethylamino)carbonyl>oxy>-3-oxo-3,6-dihydro-2H-pyran 
• 907163-79-5 6-methoxy-2--2-methyl-2H-pyran-3(6H)-one 
• 81830-85-5 6-methoxy-2--2-methyl-2H-pyran-3(6H)-one 
• 81830-86-6 methyl 2,3,6-trideoxy-5-<4-(phenylsulfonyl)phenyl>-α-DL-glycero-hex-2-enopyranosid-4-ulose 
• 145371-60-4 2--2-methyl-6-<(p-nitrobenzoyl)oxy>-2H-pyran-3(6H)-one 

Relevant academic research and scientific papers

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.

Products from Furans. 3. Crystal and Molecular Structure, Proton Nuclear Magnetic Resonance, and Conformational Studies of 2-Aryl-Substituted 2-Methyl-6-hydroxy-2H-pyran-3(6H)-one Derivatives

Crystallographic studies showed that the p-(benzenesulfonyl)phenyl substituent in 2--2-methyl-6-methoxy-2H-pyran-3(6H)-one (5-B) and in 2--2-methyl-6-oxy>-2H-pyran-3(6H)-one (4