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

Authors
Citation
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
Citations number
35
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear
ISSN journal
0022328X
Volume
508
Issue
1-2
Year of publication
1996
Pages
219 - 225
Database
ISI
SICI code
0022-328X(1996)508:1-2<219:OTC.SO>2.0.ZU;2-L
Abstract
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.