The first generation and trapping of a five-membered ring allene: 2-dehydro-3a,4,5,6,6a-pentahydropentalene
✍ Scribed by Fatih Algi; Recep Özen; Metin Balci
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 56 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
]octane (8) was prepared by addition of bromofluorocarbene to bicyclo[3.2.0]hept-6ene (5). Treatment of a solution of 8 in ether with MeLi in the presence of furan afforded the trapping product 11. The formation of the trapping product is consistent with the first generation of a five-membered ring allene, namely, 2-dehydro-3a,4,5,6,6a-pentahydropentalene (4), a reactive intermediate.
📜 SIMILAR VOLUMES
The complexation between D-threitol (1) and 2,4,6-[3,4-bis(bromomethyl)phenyl]boroxin (2) selectively afforded l>-threitol-l,3:2,4-bis [-3,4-(bisbromomethyl)phenylboro~tte] (4) including two six-membered rings, whose structure was identified by means of NMR and IR spectroscopy and X-ray crystallogra
## Abstract Reaction of 1‐amino‐3‐arylpyrido[1,2‐__a__]benzimidazole‐2,4‐dicarbonitrile **(1)** with dimethylformamide‐dimethylacetal (DMF‐DMA) gave **1**‐[__N,N__‐(dimethylaminomethylene)amino]‐3‐arylpyrido[1,2‐__a__]benzimidazole‐2,4‐dicarbonitrile **(2).** Compounds **(1)** reacted with triethyl