Reaction of 5,6-Dihydroxy-2,2,9,9-tetramethyl-4,6-decadiene-3,8-dione witho-Aminophenol ando-Aminothiophenol
โ Scribed by V. O. Kozminykh; N. M. Igidov; E. N. Kozminykh
- Book ID
- 111545165
- Publisher
- Springer US
- Year
- 2003
- Tongue
- English
- Weight
- 108 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0009-3122
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
The title compound, C 23 H 25 BrO 3 , was synthesized by the reaction of p-bromobenzaldehyde with dimedone and HClO 4 / SiO 2 in EtOH. In the molecule, the dihydropyran ring adopts a boat conformation and the two cyclohexene rings are in a trans conformation.
In the title compound, C~20~H~25~N~3~O~5~S, the pyrrolidine ring is __trans__-fused to the dihydropyran ring. The pyrrolidine ring adopts a twist conformation and the dihydropyran ring is in an envelope conformation. The tosyl group is attached to the pyrrolidine ring in a biaxial position and its b