Muriel Durandetti
Research Subjects
Muriel Durandetti has a total of 4 co-authors. Here are the top co-authors by number of shared publications:
Jacques Périchon
4 shared publicationsClothilde Meignein
Laboratoire d’Electrochimie, Catalyse et Synthèse Organique, CNRS, UMR 7582, Université Paris 12, 2 rue Henri-Dunant, 94320 Thiais, France
1 shared publicationClotilde Meignein
Laboratoire d'Electrochimie, Catalyse et Synthèse Organique, UMR 7582 CNRS, 2 rue Henri-Dunant, 94320 Thiais, France
1 shared publicationJean-Yves Nédélec
Laboratoire d'Electrochimie, Catalyse et Synthèse Organique, CNRS, UMR 7582, Université Paris 12, 2 rue Henri-Dunant 94320 Thiais, France
1 shared publication
Latest Publications
- 2 November 2004
- Published by Georg Thieme Verlag KG in Synthesis
- Vol. 2004 (18) , 3079-3083
Nickel-Catalyzed Electrochemical Coupling of Aryl, Heteroaryl or Vinyl Halides with Activated Alkyl Chlorides: Synthetic and Stereochemical Aspects
We report coupling reactions of aryl, heteroaryl or vinyl halides with activated alkyl halides, using nickel catalysis combined with an electrochemical process. Synthetic and stereochemical aspects are presented. This minireview highlights electrosynthesis in the field of synthesis and catalysis.
- 2 November 2004
- Published by Georg Thieme Verlag KG in Synthesis
- Vol. 2004 (18) , 3079-3083
Nickel-Catalyzed Electrochemical Coupling of Aryl, Heteroaryl or Vinyl Halides with Activated Alkyl Chlorides: Synthetic and Stereochemical Aspects
We report coupling reactions of aryl, heteroaryl or vinyl halides with activated alkyl halides, using nickel catalysis combined with an electrochemical process. Synthetic and stereochemical aspects are presented. This minireview highlights electrosynthesis in the field of synthesis and catalysis.
- 13 March 2003
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 68 (8) , 3121-3124
Iron-Catalyzed Electrochemical Allylation of Carbonyl Compounds by Allylic Acetates
Homoallylic alcohols were synthesized from aldehydes or ketones and allylic acetates, using an electrochemical process catalyzed by iron complexes. We first studied the reactivity of allyl acetate, using N,N-dimethylformamide (DMF) or acetonitrile (AN) as solvent, FeBr2 as catalyst, and Fe as the sacrificial anode. Then we tested the regioreactivity of crotyl acetate and other allylic derivatives.
- 13 March 2003
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 68 (8) , 3121-3124
Iron-Catalyzed Electrochemical Allylation of Carbonyl Compounds by Allylic Acetates
Homoallylic alcohols were synthesized from aldehydes or ketones and allylic acetates, using an electrochemical process catalyzed by iron complexes. We first studied the reactivity of allyl acetate, using N,N-dimethylformamide (DMF) or acetonitrile (AN) as solvent, FeBr2 as catalyst, and Fe as the sacrificial anode. Then we tested the regioreactivity of crotyl acetate and other allylic derivatives.
- 11 January 2003
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 5 (3) , 317-320
Iron-Mediated Electrochemical Reaction of α-Chloroesters with Carbonyl Compounds
[reaction: see text] Reformatsky-type reactions have been performed efficiently using an electroassisted iron-complex catalysis. Valuable product such as beta-hydroxyesters, ketones or nitriles are thus prepared with high yields.
- 11 January 2003
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 5 (3) , 317-320
Iron-Mediated Electrochemical Reaction of α-Chloroesters with Carbonyl Compounds
[reaction: see text] Reformatsky-type reactions have been performed efficiently using an electroassisted iron-complex catalysis. Valuable product such as beta-hydroxyesters, ketones or nitriles are thus prepared with high yields.
- 1 June 2001
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 3 (13) , 2073-2076
An Electrochemical Coupling of Organic Halide with Aldehydes, Catalytic in Chromium and Nickel Salts. The Nozaki−Hiyama−Kishi Reaction
Electrochemical arylation of arenecarboxaldehydes using an iron sacrificial anode in the presence of chromium and nickel catalysts afforded the corresponding arylated secondary alcohols in moderate to good yields. The chromium and nickel salts as catalysts are obtained by oxidation of a stainless steel rod during a preelectrolysis in 7% and 3%, respectively. The process was also applied to the addition of vinyl halide, allyl acetate, or α-chloroester to aromatic aldehydes.
- 1 June 2001
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 3 (13) , 2073-2076
An Electrochemical Coupling of Organic Halide with Aldehydes, Catalytic in Chromium and Nickel Salts. The Nozaki−Hiyama−Kishi Reaction
Electrochemical arylation of arenecarboxaldehydes using an iron sacrificial anode in the presence of chromium and nickel catalysts afforded the corresponding arylated secondary alcohols in moderate to good yields. The chromium and nickel salts as catalysts are obtained by oxidation of a stainless steel rod during a preelectrolysis in 7% and 3%, respectively. The process was also applied to the addition of vinyl halide, allyl acetate, or α-chloroester to aromatic aldehydes.