The reaction proceeds through a radical mechanism, with the alkene activation step generating radicals on the alkene. The radicals can then react with the alcohol and the aryl coupling partner to form the desired product.
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hexa-2,3-diene-1,6-diyldibenzene
acetic acid 2-(diphenyl-phosphinoyl)-1-methyl-but-3-enyl ester
1,4-Naphthalenedione, 2-acetyl-3-(2-propenyl)-
2-azido-1-iodo-1-phenylcyclohexane
((1S,2R,3S,4R)-1-Benzyl-4-tert-butoxycarbonylamino-2,3-dihydroxy-5-phenyl-pentyl)-carbamic acid tert-butyl ester
2-(1-p-tolylbut-3-enyl)malononitrile
1H-Pyrrole, 2,3-diphenyl-
4-NITROPHENYLOXAMIC ACID
6-methyl-3-(trifluoromethyl)-2H-1-benzopyran-2-one
(E)-N-(3-(2-nitrovinyl)phenyl)tetradecanamide
4-benzyl-4-methoxycyclohexa-2,5-dienone
[2,2,2-Trifluoro-1-(trifluoromethyl)ethyl]benzene
