The Journal of Organic Chemistry

Substituent effects on excited-state efficiencies: thermolysis of 3, 3-(2, 2'-biphenyldiyl)-4-methyl-4-aryl-1, 2-dioxetanes

WH Richardson, SA Thomson

Index: Richardson, William H.; Thomson, Stephen A. Journal of Organic Chemistry, 1985 , vol. 50, # 11 p. 1803 - 1810

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Citation Number: 14

Abstract

Results Synthesis and Product Studies. The classical synthetic route to dioxetanes was employed, ie, olefin to P-bromo hydroperoxide (BHP) to di~ xetanes.~ The olefins were prepared from cross-coupling of fluorenone with the acetophenones with low-valent titanium, with one exception. For 3 (Ar= 3, 4-(CH3) 2C6H3 and p-BrC6H4), the McMurry procedure was used, where titanium trichloride was reduced with lithi~ m.~ With one ...

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