(SIGMA-ALKYL)IRON COMPLEXES AS INTERMEDIATES IN (PORPHINATO)IRON-MEDIATED REDUCTION OF ALKENES AND ALKYNES WITH SODIUM-BOROHYDRIDE

Authors
Citation
M. Takeuchi et K. Kano, (SIGMA-ALKYL)IRON COMPLEXES AS INTERMEDIATES IN (PORPHINATO)IRON-MEDIATED REDUCTION OF ALKENES AND ALKYNES WITH SODIUM-BOROHYDRIDE, Organometallics, 12(6), 1993, pp. 2059-2064
Citations number
36
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear
Journal title
ISSN journal
02767333
Volume
12
Issue
6
Year of publication
1993
Pages
2059 - 2064
Database
ISI
SICI code
0276-7333(1993)12:6<2059:(CAII(>2.0.ZU;2-H
Abstract
The (porphinato)irons promote the reduction of alkenes and alkynes wit h NaBH4 in anaerobic benzene-ethanol. Styrene is reduced to 2,3-diphen ylbutane and ethylbenzene, whose precursors have been assumed to be th e (sigma-alkyl)iron(III) and -iron(II) porphyrin complexes, respective ly. The (sigma-alkyl)iron(III) porphyrin complex has the reactivity of the alkyl radical while the (sigma-alkyl)iron(II) porphyrin complex s hows the nature of the carbanion.