Tetracyclo[5.1.0.01,6.02,7]octane: some unexpected addition reactions and a new synthesis
✍ Scribed by Johannes Belzner; Günter Szeimies
- Book ID
- 104227717
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 217 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract Alkalische Zersetzung der bis‐__p__‐Toluol‐sulfonylhydrazone **3** und **4** von sowohl __anti__‐ (**1**) wie auch __syn__‐Bis‐homo‐__p__‐chinon (**2**) ergab 4,5‐Homo‐1,7‐diaza‐inden (**5**). Das Produkt hat Eigenschaften eines Pyrazols und eines Olefins. Durch katalytische Reduktion e
Condensation of different cyclic ketones with visnaginone la and khellinone lb afforded spirofurochromanone derivatives 2a-f. Compounds 2a and 2b were readily demethylated to give the compounds 3a and 3b. Nitration of 2b and 2e gave the nitrofurochromonone and quinone derivatives 4 and 5 respectivel
Synthesis and Reactions of Some New Benzimidazoles. Part 2. -Starting from known, biologically active compounds of type (III) various modifications are carried out to test new types of compounds for their antimicrobial activity. Compounds (VI), (VIIIa), and (XI) show moderate activity against Pseud
We found no indication for the intermediate formation of diazo compounds (cf. [14]).