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Bakkane

Cannon. Taiho, Kaho, Kanoho Cap (explosive). Bakkan Carbine. Kiju... [Pg.466]

Combustion. Nensho Danto bakkan. Point Detonating Fuze... [Pg.468]

Cyclotol (50/50—RDX/TNT). Chauyaku Denki bakkan. Electric Primer... [Pg.468]

Detonating Fuze. Shinkan Bakkan Eikodan. Tracer Bullet... [Pg.471]

Dokasaku. Safety Fuse Powder Train Electric Primer. Denki bakkan... [Pg.471]

Denki bakkan. Electric Primer Denki ratkan. Electric Cap... [Pg.468]

Tenka bakkan. Igniting Primer Tenka shinkan. Igniting Fuze Tenkayaku. Igniting Charge Terumitto (Thermite). See Shakunetsuzai Terumitto shoidan. Thermite Bomb Teryudan. Tenagedan Tessen keitei. Trip Wire... [Pg.503]

The Staudinger ketene cycloaddition was utilized as the key reaction in the synthesis of a number of bakkane natural products in the laboratory of A.E. Greene. Dichloroketene was generated in situ from trichloroacetyl chloride by zinc-copper alloy in the presence of phosphorous oxychloride. The [2+2] cycloaddition between dichloroketene and 1,6-dimethylcyclohexene gave the product in high yield and excellent regio- and diastereoselectivity. The cycloadduct was successfully converted to (+)-bakkenolide A. [Pg.427]

Evans stereoselective synthesis of the bakkane sesquiterpene bakkenolide A (212) showcased a powerful related [2,3]-rearrangement (Scheme 16.27) [112]. After deprotonation, the allylic carbazate 210 underwent thermal decomposition to form a carbene. This participated in a [2,3]-rearrangement from the more sterically accessible convex face of the bicyclic system, thus generating the quaternary stereogenic center in product 211. [Pg.538]

See other pages where Bakkane is mentioned: [Pg.111]    [Pg.462]    [Pg.463]    [Pg.470]    [Pg.482]    [Pg.487]    [Pg.494]    [Pg.504]    [Pg.462]    [Pg.463]    [Pg.470]    [Pg.482]    [Pg.487]    [Pg.494]    [Pg.504]    [Pg.684]    [Pg.767]    [Pg.1414]   
See also in sourсe #XX -- [ Pg.427 ]



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Eremophilane, Bakkane (Fukinane), Ishwarane

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