The discovery' that bicycle [ 5.1.01 o&a-2, S-diene (3,4-hometropilidene, I) undergoes a rapidly reverisible, degenerate Cope roarrangement has stimulated considerable theoretical interest. The generality of such behavior hae recently been put to test by the Syntheal11 of trtcyclo [ 3.3.2. 04' 6] de
Photocycloaddition reactions of tricyclo[3.3.1.02,8]nona-3,6-dien-9-one (barbaralone) and carbonyl compounds
β Scribed by Tsutomu Miyashi; Akinori Konno; Yasutake Takahashi; Atsuko Kaneko; Takanori Suzuki; Toshio Mukai; Noboru Koga; Hiizu Iwamura
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- French
- Weight
- 279 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0040-4039
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Recently, Cargill and coworkers1 have reported that irradiation of antitricyclo[5.2.0.0 285]nona-3,8-dien-9-one(I)l'2 in methylenechloride with "black-CI, lights" gives homocubane as a major product. However, it may be expected that
The rhodium(II)-catalyzed diazo decomposition of 7-diazocarbonyltethered-l,3,5-cycloheptatriene 3 generated tricyclic ketoester 4 in 64% yield. Reaction of ketoester 4 with nucleophiles leads to cyclopropane cleavage (Nu --PhSNa) to give 5 or rearrangement (Nu = RNH2) to give 7 or 8.
## Abstract Alkylation of 4,4,6βtrimethylβ2βcyclohexenone (**1**) in toluene in the presence of sodium bis(trimethylsilyl)amide proceeds smoothly to give high yields of compounds **2**. Irradiation (Ξ»= 366 nm) of the 6βallylβ4,4,6βtrimethylβ2βcyclohexenones **2aβc** yields mixtures of the isomeric
## Abstract The first preparation of title compound **1** is accomplished. Its heterocyclic structure was characterized spectroscopically and by Xβray structure analysis.