Mesoionic compounds. 10. Preferred conformation of a 3-alkyl and 3-aryl-substituent in 4-unsubstituted and 4-acylated monocyclic munchnones and sydnones
H. Petride et al., Mesoionic compounds. 10. Preferred conformation of a 3-alkyl and 3-aryl-substituent in 4-unsubstituted and 4-acylated monocyclic munchnones and sydnones, REV RO CHIM, 44(3), 1999, pp. 249-259
A new 4-unsubstituted monocyclic oxazolium-5-olate (7c) was generated and N
MR-characterized. Several 3-alkyl- and 3-aryl-4-acylated monocyclic munchno
ne and sydnone derivatives were also prepared. From NMR experimental data a
nd theoretical calculations different conformations were proposed for the 3
-alkyl group in munchnone- and sydnone series. The 3-arylated mesoionic oxa
zolones presented non-planar structures.