Thermal cycloaddition to cis, cis, cis, cis-1,3,5,7-cyclononatetraene
β Scribed by A.G. Anastassiou; R.P. Cellura
- Publisher
- Elsevier Science
- Year
- 1970
- Tongue
- French
- Weight
- 190 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
80 "C/0.003 Torr; UV-Spektrum (in n-Hexan): 302 (4.17), 270 (4.12), 260 (4.06) nm (log E ) ; NMR-Spektrum (in CDC13): Dublett zentriert bei 7 = 7.34 (4CH3). Multipletts zentriert bei T = 6.17 (H-3a, H-7a), bei 4.55 (H-2. H-3. H-4, H-5, H-6) und bei 3.65 (H-7)]. Das NMR-Spektrum von (5) erlaubt keine
Table I. Properties of sugar esters of substituted stearic acids (SSE) I I I 2.20 2.26 2.36 Compound 2.20 2.13 2.18
It was reported recently (3) from this Laboratory that cis-cis-cis-1,4,7-cyclononatriene I is isomerized by potassium t-butoxide (KOBu) in dimethylsulfoxide (DMSO) to the cis-cis-cis-1,3,6:isomer 11 and then to the bicyclic isomer, (4) cis-bicyclo[4. 3.O]nona-P, rl-diene IV. Although cis-cis-cis-1,3