Various unstrained sec-alcohols, including cycloalkanols, reacted with alke
nes under a catalytic system of Rh(I) complex, 2-amino-3-picoline, and K2CO
3 to give the alkyl-group-exchanged ketones through transfer hydrogenation
and consecutive carbon-carbon bond activation The presence of base is essen
tial to enhance the rate of the oxidation step, and alkene acts as a hydrog
en acceptor and a substrate of the carbon-carbon coupling reaction.