2,5-Dihydro-4-hydroxymethyl-1,3-oxazoles by Asinger condensation
✍ Scribed by Alexander Dömling; Angela Bayler; Ivar Ugi
- Book ID
- 107857441
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 237 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The title compound, [Fe(C~5~H~5~)(C~9~H~10~NO~2~)], was prepared from ferrocenecarboxylic acid and serine. In the crystal structure, molecules are arranged in chains with an intermolecular hydrogen bond between hydroxy groups and N atoms.
The title compound, C~20~H~17~NO~6~, was synthesized by the reaction of syringaldehyde with hippuric acid. The molecule adopts a __Z__ configuration about the central olefinic bond. The two benzene rings and the oxazolone ring are almost coplanar. The crystal structure is stabilized by weak intermol
2,3-Diphenyl-2,3-dihydrospiro[1,3-oxazole-5(4H),1 0 0 0 (3 0 0 0 H)-2-benzofuran]-3 0 0 0 -one