OPTICALLY-ACTIVE TRANSITION-METAL COMPLEXES .3. SYNTHESIS OF OPTICALLY-ACTIVE (ETA(4)-AMINODIOLEFIN) TRICARBONYL IRON COMPLEXES - KINETIC RESOLUTION OF A CHIRAL AMINE BY MEANS OF AN OPTICALLY-ACTIVE DIENYL IRON CATION
M. Kaser et A. Salzer, OPTICALLY-ACTIVE TRANSITION-METAL COMPLEXES .3. SYNTHESIS OF OPTICALLY-ACTIVE (ETA(4)-AMINODIOLEFIN) TRICARBONYL IRON COMPLEXES - KINETIC RESOLUTION OF A CHIRAL AMINE BY MEANS OF AN OPTICALLY-ACTIVE DIENYL IRON CATION, Journal of organometallic chemistry, 508(1-2), 1996, pp. 219-225
The synthesis of optically active eta(4)-(aminodiolefin)tricarbonyl ir
on complexes by the nucleophilic addition of primary and secondary ami
nes to the optically active ricarbonyl-(1R)-(eta(5)-methyl-nopadienyl)
iron(1+) cation (4) is described. Under either kinetic or thermodynami
c control, the reaction leads to (E,Z)- or (E,E)-diolefin complexes wi
th generation of a new chiral carbon centre. Racemic (R/S)-phenylethyl
amine was kinetically resolved (de=38%) by treatment with 4 at -78 deg
rees C.