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Iron-Catalyzed Reduction and Hydroelementation Reactions

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Iron Catalysis II

Part of the book series: Topics in Organometallic Chemistry ((TOPORGAN,volume 50))

Abstract

During the last two decades, iron has proved to be an interesting transition metal which is a highly valuable alternative to classical precious ones for catalyzing organic transformations including the reduction of unsaturated C–C or C–heteroatom bonds. This chapter summarizes the rapid development of iron catalyzed selective reductions of alkene, alkyne, carbonyl and carboxylic derivatives. The emerging topic of hydroboration of alkenes and alkynes is also described.

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Abbreviations

cat:

Catechol

cod:

1,5-Cyclooctadiene

Cp:

Cyclopentadienyl

dcpe:

1,2-Bisdicyclohexylphosphinoethane

DBU:

1,8-Diazabicyclo[5.4.0]undec-7-ene

DFT:

Density functional theory

Dipp:

2,6-Diisopropylphenyl

DMC:

Dimethyl carbonate

DRA:

Direct reductive amination

EDTA-Na2 :

Ethylenediaminetetraacetic acid disodium salt

IMes:

1,3-Bis(2,4,6-trimethylphenyl) imidazole-2-ylidene

IPr:

1,3-Bis(2,6-diisopropylphenyl) imidazole-2-ylidene

MD’M:

[(MeO)2MeSiH]

Mes:

2,4,6-Trimethylphenyl

NHC:

N-Heterocyclic carbene

NPs:

Nanoparticles

pin:

Pinacol

PMHS:

Polymethylhydrosiloxane

t-PBO:

trans-4-Phenyl-but-3-en-2-one

terpy:

2,2′:6′,2″-Terpyridine

TFA:

Trifluoroacetic acid

TMDS:

1,1,3,3-Tetramethyldisiloxane

TMEDA:

N,N,N′,N′-Tetramethylethylenediamine

TMPP:

Tris(2,4,6-trimethoxyphenyl)phosphine

TOF:

Turnover frequency

TON:

Turnover number

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Darcel, C., Sortais, JB. (2015). Iron-Catalyzed Reduction and Hydroelementation Reactions. In: Bauer, E. (eds) Iron Catalysis II. Topics in Organometallic Chemistry, vol 50. Springer, Cham. https://doi.org/10.1007/3418_2015_104

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