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Photopericyclic reactions

Unlike other diene photopericyclic reactions, cyclohexadiene ring opening proceeds with reasonable efficiency in phenyl-substituted derivatives, although the quantum yields are generally significantly lower than those of non-arylated systems. Two examples of the conversion of 93 to 94 are shown in equation 36178,179... [Pg.225]

See other pages where Photopericyclic reactions is mentioned: [Pg.197]    [Pg.197]    [Pg.197]    [Pg.199]    [Pg.201]    [Pg.203]    [Pg.209]    [Pg.211]    [Pg.212]    [Pg.212]    [Pg.213]    [Pg.215]    [Pg.217]    [Pg.219]    [Pg.221]    [Pg.223]    [Pg.225]    [Pg.227]    [Pg.229]    [Pg.231]    [Pg.231]    [Pg.233]    [Pg.235]    [Pg.237]    [Pg.239]    [Pg.241]    [Pg.243]    [Pg.245]    [Pg.247]    [Pg.249]    [Pg.251]    [Pg.253]    [Pg.256]    [Pg.1201]    [Pg.197]    [Pg.197]    [Pg.197]    [Pg.201]    [Pg.203]    [Pg.209]    [Pg.212]    [Pg.213]    [Pg.215]    [Pg.217]    [Pg.219]    [Pg.223]    [Pg.225]   


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Conjugated diene complexes photopericyclic reactions

Photopericyclic reactions of conjugated dienes

Photopericyclic reactions of conjugated trienes

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