Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Cycloocta-1,5-diynes

The through-bond conjugation with strong ct-tt mixing for tetrasila-cycloocta-l,5-diyne is further demonstrated by photoelectron spectroscopic (15) and ab initio (3-21G basis set) studies (16). [Pg.362]

Coupling reactions. The hexacarbonyldicobalt complexes of cycloocta-l,5-diynes and cyclooct-3-ene-l,5-diynes have been acquired by reductive cyclization of the dication... [Pg.404]

Octa-l,7-diene-3,5-diyne hydrogenated with Lindlar catalyst in n-hexane containing quinoline at 24-25° and slightly more than atmospheric Hg-pressure cycloocta-l,3,5-triene. Y 80%. W. Ziegenbein, B. 98, 1427 (1965). [Pg.471]


See other pages where Cycloocta-1,5-diynes is mentioned: [Pg.362]    [Pg.362]    [Pg.362]    [Pg.539]    [Pg.386]    [Pg.869]    [Pg.197]    [Pg.246]    [Pg.405]    [Pg.179]    [Pg.179]    [Pg.180]    [Pg.362]    [Pg.34]    [Pg.287]    [Pg.114]    [Pg.114]   
See also in sourсe #XX -- [ Pg.404 ]




SEARCH



Cycloocta

Diynes

© 2024 chempedia.info