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Longibornanes

An important characteristic of medium-sized alicyclic rings is the ease with which transannular reactions arising from proximity of atoms occur (e.g. see 103). In the preferred conformation of the four-carbon bridge in the longifolane (155) and longibornane (156) systems, the proximity of the C-3, C-10 and C-2, C-9 positions, respectively has been responsible for interesting transannular reactions, both of homolytic and heterolytic types. [Pg.82]


See other pages where Longibornanes is mentioned: [Pg.39]    [Pg.85]    [Pg.89]    [Pg.103]    [Pg.180]    [Pg.137]    [Pg.741]    [Pg.73]    [Pg.149]    [Pg.39]    [Pg.85]    [Pg.89]    [Pg.103]    [Pg.180]    [Pg.137]    [Pg.741]    [Pg.73]    [Pg.149]   
See also in sourсe #XX -- [ Pg.82 , Pg.84 , Pg.85 ]

See also in sourсe #XX -- [ Pg.149 ]




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Longibornane

Longibornanes, and Longifolanes

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