Five xyoctahydro-7.8,8-trimethyl-4,7-methanobenzofurans were tested as
additives for the enantioselective addition of butyllithium and butyl
magnesium bromide to benzaldehyde. The selectivity of the reaction was
determined by GC. HPLC, and by measurement of the optical rotation of
the obtained 1-phenyl-1-pentanol, and the stability of the ligands un
der the given reaction conditions was investigated. Upon reaction with
benzaldehyde, the addition of -2-(2-(phenylmethoxy)ethoxy)-4,7-methan
obenzofuran to butylmagnesium bromide yielded (R)-1-phenyl-1-pentanol
with 47% ee.