A stereoselective decarboxylation of 1,6-dimethyl-3-(3′-indolyl)methyl-3-carboxy-2,5-piperazinedione
✍ Scribed by Yoshito Kishi; Shinichi Nakatsuka; Tohru Fukuyama; Toshio Goto
- Publisher
- Elsevier Science
- Year
- 1971
- Tongue
- French
- Weight
- 183 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
In connection with synthetic study on the carboxylic acids (Ia) and (Ib) as synthetic
📜 SIMILAR VOLUMES
In the title compound, C 24 H 20 N 4 S, the phenyl ring forms a dihedral angle of 49.22 (7) with the indole ring system. The indole and benzothiazole ring systems are both approximately planar, with dihedral angles between the five-and sixmembered rings of 0.98 (7) and 1.28 (5) , respectively. They
The title compound, C 26 H 23 N 3 O 8 , is a nefidipine analogue. The dihydropyridine ring has a flattened boat conformation. No hydrogen bonds exist in the crystal packing.