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Functionalized ketones by iron mediated reaction of grignard reagents with acyl chlorides

✍ Scribed by C. Cardellicchio; V. Fiandanese; G. Marchese; L. Ronzini


Publisher
Elsevier Science
Year
1987
Tongue
French
Weight
219 KB
Volume
28
Category
Article
ISSN
0040-4039

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✦ Synopsis


The iron(:II)-catalyzed cross-coupling reaction between Grignard reagents and acyl ___chlorides was found to be widely applicable to the synthesis of various functionalized ketones in good yields under mild conditions; the series of examples includes the synthesis of chiral methyl ketones and symmetric diketones.

In a previous work', we have reported a simple and versatile synthesis leading to ketones in high yields and without concomitant formation of alcohols.

The procedure involves a


πŸ“œ SIMILAR VOLUMES


Iron catalyzed cross-coupling reactions
✍ V. Fiandanese; G. Marchese; V. Martina; L. Ronzini πŸ“‚ Article πŸ“… 1984 πŸ› Elsevier Science 🌐 French βš– 197 KB

TABLE Cross-Coupling Reactions of Acyl Chlorides with Grignard Reagents in the Presence of Fe(acac)3 as a Catalysta. R-C+ 0 3% Fe(acac)3 0 + 'Cl R'MgXb THF R-C< R' Entry R R' Temp Yield in KetoneC % 1 CH3(Ct& CH3 r.t. 84 2 CH3(CH2)4 CH3(C"2)4 r.t. 82 3 CH3 CH3(CH2)8 r.t. 82 4 CH3 CH3(CH2)9 r.t. 80 5

ChemInform Abstract: Reactions of Acyl T
✍ H. MAEDA; K. TAKAHASHI; H. OHMORI πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 32 KB πŸ‘ 1 views

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