## Abstract Starting from 3,3′‐bi‐indenyle and 1,4‐naphthoquinone the title compound, III, has been synthesized in 3 steps (overall yield 54.6%).
Identification spectroscopique du diméthyl-1,2-dihydro-1,2-anthracène
✍ Scribed by R. Gerdil; E. A. C. Lucken
- Publisher
- John Wiley and Sons
- Year
- 1961
- Tongue
- German
- Weight
- 213 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Aprks une distillation fractionnbe d'un Cchantillon huileux obtenu 2 partir de la deuxieme fraction de la chromatographie (benzknc) et des crijtalli ;ations r6p&es, on a isold un hydrocarbure anthrachnigue, rest6 non identifie (VIII) : paillettes fluorescentcs, F. 126-127,5" (mdthanol).
C,,H,, (290,45)
Calc. C 90,98 H 9,02.,6 Tr. C 91,38 H S,Sl% Environ 20 ml de gaz se sont d6gagCs pendant la rdaction et ont Lt6 identifigs comme &ant de I'isobuthe par chromatographie en phase gazeuse.
📜 SIMILAR VOLUMES
## Abstract Benzocyclobutene **10** and 3‐oxabicyclo [3.2.0]hepta‐1, 4‐diene **11** are formed by gas‐phase pyrolysis of the title compound **9**. The results are discussed with reference to the estimated reaction parameters. It is found that the activation due to oxygen in **9** is relatively weak
## Abstract 3,8‐Dimethyl‐2,7‐nonadienoic acid has been prepared. Its structure corresponds to that of geranic acid with the only difference that it contains an additional CH~2~‐group in the middle of the chain. By the action of a mixture of formic and sulfuric acids a cyclic isomer, analogous to α‐