81830-87-7Relevant academic research and scientific papers
Stereoselective Ring Closure of 6-oxy>-2H-pyran-3(6H)-ones. Formation of the 5H-Pyranooxazole-2,6-dione Ring System
Georgiadis, Minas P.,Couladouros, Elias A.
, p. 1757 - 1760 (2007/10/02)
The stereospecific formation of the 5H-pyranooxazole-2,6-dione ring system from 2,2-disubstituted 6-oxy>-2H-pyran-3(6H)-one via an enolization at C-5 is presented.The outcome of the same reaction in the case of 2-monosubstit
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
Georgiadis, Minas P.,Couladouros, Elias A.,Polissiou, Moschos G.,Filippakis, S. E.,Mentzafos, D.,Terzis, A.
, p. 3054 - 3058 (2007/10/02)
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
