## Abstract Starting from 5‐benzoyl‐2,4‐dibromobenzoic acid and 3‐methyl‐fluorene, the 6‐methyl‐9,15‐dihydro‐__7H__‐diindeno[2.1‐__b__; 2′,1′‐__g__]fluorene, a derivative of a mono‐angular diindenofluorene has been synthesized in 5 steps (overall yield 1,5%).
Synthèses dans la série des bis-indéno-fluorènes, IX. Le dihydro-13,15-7H-bis-indéno[2.1-b; 2′.1′-h]fluorène et son dérivé méthylé en position 6
✍ Scribed by Louis Chardonnens; Jean-Luc Barras
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- German
- Weight
- 440 KB
- Volume
- 57
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
By condensation according Ullmann of 2‐iodo‐9‐oxo‐fluorene with 3‐bromo‐2‐cyano‐9‐oxo‐fluorene, followed by cyclisation and reduction, the new linear 13,15‐dihydro‐7H‐diindeno[2.1‐b; 2′.1′‐h]fluorene (III) is synthesized in 3 steps. The 6‐methyl‐derivative of II is also obtained in a similar way.
📜 SIMILAR VOLUMES
## Abstract Starting from 3, 4‐dimethylfluorene the title compound, 5, 6‐dimethyl‐7, 12‐dihydro‐indeno[1,2‐a]fluorene (IV), is synthesized in four steps (overall yield 9%). The same hydrocarbon is also obtained in four steps starting from the phthalaconecarboxylic acid of __Gabriel__. This corrobor
Ill] AECKERT & F.SEIDEL, J. prakt. Chem. [2] 102, 358 (1921).