Synthesis of γ-ketocarboxylic acids via reduction of γ-keto-α-hydroxycarboxylic acids with carbon monoxide catalyzed by a PdHCl system
TLDR
In this paper, the catalytic cycle proceeds through the following steps: (i) the chloride ArCOCH2CHClCOOH, which forms in situ from the starting substrate and HCl, undergoes oxidative addition to reduced palladium with formation of a catalytic intermediate having a Pd-[CH(COO H)CH2COPh] moiety.About:
This article is published in Journal of Molecular Catalysis.The article was published on 1994-04-20 and is currently open access. It has received 8 citations till now. The article focuses on the topics: Palladium & Catalytic cycle.read more
Citations
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Catalytic conversions in water. Part 4: Carbonylation of 5-hydroxymethylfurfural (HMF) and benzyl alcohol catalysed by palladium trisulfonated triphenylphosphine complexes
TL;DR: In this article, the authors used the water soluble catalyst Pd(TPPTS)3 (TPPTS = sodium salt of trisulfonated triphenylphosphine, P(C6H4-m-SO3Na)3) for renewable 5-hydroxymethylfurfural (HMF) carbonylation.
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TCA Cycle Involved Enzymes SucA and Kgd, as well as MenD: Efficient Biocatalysts for Asymmetric C–C Bond Formation
TL;DR: Asymmetric mixed carboligation reactions of α-ketoglutarate with different aldehydes were explored with the thiamine diphosphate dependent enzymes SucA, Kgd and MenD to selectively deliver chiral δ-hydroxy-γ-keto acids with moderate to excellent stereoselectivity.
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A sustainable procedure toward alkyl arylacetates: palladium-catalysed direct carbonylation of benzyl alcohols in organic carbonates
TL;DR: In this article, a sustainable procedure for the synthesis of various alkyl arylacetates from benzyl alcohols has been developed, with palladium as the catalyst and organic carbonates as the green solvent and in situ activator.
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Tailoring the S‐Selectivity of 2‐Succinyl‐5‐enolpyruvyl‐6‐hydroxy‐3‐cyclohexene‐1‐carboxylate Synthase (MenD) from Escherichia coli
Robert Westphal,Doris Hahn,Ursula Mackfeld,Simon Waltzer,Maryam Beigi,Michael Widmann,Constantin Vogel,Jürgen Pleiss,Michael Müller,Dörte Rother,Martina Pohl +10 more
TL;DR: Opening the S‐pocket and simultaneous destabilization of the R‐pathway provides a potential general new strategy to enhance the S-selectivity of ThDP‐dependent enzymes.
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Palladium catalyzed hydrodechlorination of α-chloroacetophenones by hydrogen transfer from the H2OCO system
TL;DR: In this paper, it was shown that PdCl2(PPh3)2 is an excellent catalyst precursor for the hydrodechlorination of α-chloroacetophenone to acetophenone by hydrogen transfer from the H2OCO system.
References
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Organic Syntheses by Means of Noble Metal Compounds. VIII.1 Catalytic Carbonylation of Allylic Compounds with Palladium Chloride
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Palladium-catalyzed decarboxylation-carbonylation of allylic carbonates to form β,γ-unsaturated esters
TL;DR: La decarboxylation-carbonylation de (allyl alkyl) carbonates en les esters alkylsiques d'acides aliene-3oiques, se fait par reaction avec le monoxyde de carbone en presence de complexes de palladium coordines a des phosphines tertiaires as discussed by the authors.
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Noble metal catalysis. III. Preparation of dialkyl oxalates by oxidative carbonylation
TL;DR: The Synthese von Diathyloxalat (IV) in Alkoholen unter Zusatz von Edelmetallkatalysatoren und Oxidationsmitteln wird untersucht.
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Mechanisms of double and single carbonylation reactions of aryl iodides catalyzed by palladium complexes to give .alpha.-keto esters and esters
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Arylation of Olefin with Iodobenzene Catalyzed by Palladium
TL;DR: Arylation of propylene, ethylene, styrene, and methyl acrylate with iodobenzene was found to be catalyzed by metallic palladium in methanol to give methylstyrene and methyl cinnamate, respectively as discussed by the authors.