The Photochlorination of 2-Methylpropane-2-d and α-d1-Toluene; the Question of Free Radical Rearrangement or Exchange in Substitution Reactions1,2

1952 ◽  
Vol 74 (16) ◽  
pp. 3995-3998 ◽  
Author(s):  
Herbert C. Brown ◽  
Glen A. Russell
1994 ◽  
Vol 35 (31) ◽  
pp. 5563-5566 ◽  
Author(s):  
Paul Dowd ◽  
Wei Zhang ◽  
Khalid Mahmood

1970 ◽  
Vol 92 (10) ◽  
pp. 3203-3205 ◽  
Author(s):  
Norbert. Frydman ◽  
Yehuda. Mazur

1968 ◽  
Vol 21 (6) ◽  
pp. 1571 ◽  
Author(s):  
W Davies ◽  
BC Ennis ◽  
QN Porter

It is shown that heat in the absence of a solvent converts the title compound into benzo[k,l]thioxanthen 7,7-dioxide, 7-thiabenzo[c]fluorene, and o-(1-naphthyl)-benzenesulphonic acid. From these results and a consideration of the related pyrolyses of the 3,10- and 1,8-dimethyl derivatives of the title compound, a free-radical rearrangement mechanism is proposed to explain the observations.


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