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Ketones, fused ring polycyclic

Tellurophene aldehydes and ketones readily undergo reduction reactions typical of carbonyl compounds. The Wittig reaction of 2,5-bis(dodecyloxy)- -xylene-bis(triphenylphosphonium bromide) with tellurophene-2,5-dicarbaldehyde leads to poly(2,5-tellurophenediylvinylene) (MW 7000-29000 Da) in 65% yield <1995MM8363>. The condensation reactions of 2,5-diphenyl-3,4-diformyltellurophene 15 have been employed for the synthesis of a number of bi- and polycyclic heterocycles with a fused tellurophene ring (Scheme 8) <1976CB3886>. [Pg.1014]


See other pages where Ketones, fused ring polycyclic is mentioned: [Pg.671]    [Pg.671]    [Pg.680]    [Pg.671]    [Pg.680]    [Pg.99]    [Pg.99]    [Pg.285]    [Pg.196]    [Pg.196]    [Pg.1128]    [Pg.820]    [Pg.820]    [Pg.156]    [Pg.1130]    [Pg.285]    [Pg.371]    [Pg.720]    [Pg.1130]    [Pg.101]    [Pg.514]    [Pg.136]    [Pg.460]    [Pg.98]    [Pg.198]    [Pg.155]    [Pg.91]    [Pg.171]    [Pg.106]   


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Fused rings

Ketones polycyclic

Ring Ketones

Rings Ring Ketones

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