Both (2R,5R)- and (2S,SR)-isomers of 2-chloro-2-isopropyl-5-methyl-, 2-chlo
ro-2-methyl-5-isopropyl- and 2-fluoro-2-methyl-5-isopropylcyclohexanones ha
ve been synthesized and fully characterized. It is shown that a rapid overv
iew of the H-1 NMR spectrum allows an unambiguous assignment of the axial o
r equatorial position of the halogen atom and that the IR VCO absorption do
es not differ from one isomer to the other. (C) 2000 Published by Elsevier
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