1,5-Cyclooctadien-nickel-bromid und -jodid
β Scribed by Dr. L. Porri; Dr. G. Vitulli; Dr. M. C. Gallazzi
- Publisher
- John Wiley and Sons
- Year
- 1967
- Tongue
- English
- Weight
- 139 KB
- Volume
- 79
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
13% b) und intramolekularen Cyc?opropanierungs-Produkten (14a, b). Bicyclo[6.l.0]non-4-en-9-carbonsauren sind mogliche Ausgangsstoffe fur Polycyclensynthesen uber intramolekulare Carbenadditionen '). Ein rationeller Syntheseweg zu diesen ware gegeben, wenn die Addition von Chlorcyanketen an 1,5-Cyc
Bromination of 1,5-cyclooctadiene (1) and stepwise dehydro-enyne 4 are highly reactive dienophiles. The cycloadducts bromination first with KOtBu and then with KOtBu/l8-10-14 formed with 1,3-cyclohexadiene, carbon disulfide, crown-6 yields 1,5-~yclooctadiyne (5). A prolonged interac-and tetraphenylc