5, 6, 7, 8-Tetrahydro-indanon-(5)
✍ Scribed by V. Prelog; M. Zimmermann
- Publisher
- John Wiley and Sons
- Year
- 1949
- Tongue
- German
- Weight
- 244 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Das bisher unbekannte 5, 6, 7, 8‐Tetrahydro‐indanon‐(5) wurde in drei Reaktionsstufen aus Cyclopentanon‐(2)‐carbonsäure‐(1)‐äthylester und γ‐Chlor‐crotyl‐chlorid hergestellt.
📜 SIMILAR VOLUMES
The selenious acid oxidation of 2-aryl-7,7-dimethyl-5,6,7,8-formation of an intramolecular unsymmetrical diselenide by selenious acid oxidation and reports the first derivatives of tetrahydro-5-quinazolones 2a-c leads to the corresponding 2-aryl-7,7-dimethyl-6,8-epidiseleno-5,6,7,8-tetrahydro-5-the
**Notes on the Synthesis of Sulfonated Derivatives of 5,6,7,8‐Tetrahydro‐1‐naphthylamine and 5,6,7,8‐Tetrahydro‐2‐naphthylamine** Sulfonation of 5,6,7,8‐tetrahydro‐1‐naphthylamine (**1**) with sulfuric acid gave a mixture of 1‐amino‐5,6,7,8‐tetrahydronaphthalene‐2‐sulfonic acid (**2**), 4‐amino‐5,6
## Abstract __N__‐(2‐Amino‐5,6,7,8‐tetrahydro‐6‐quinazolinyl)acetamide (**9**) and __N__‐(2,4‐diamino‐5,6,7,8‐tetrahydro‐6‐quinazolinyl)acetamide (**6**) were synthesized from __N__‐(4‐oxocyclohexyl)acetamide (**5**) as novel peptidomimetic building blocks. With similar purpose, __N__‐(6‐oxo‐5,6,7,