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Recherche sur les produits chimiques et la synthèse personnalisée

Les membres du département de recherche de Georganics participent activement à la recherche en chimie organique au niveau académique/universitaire. Nous nous intéressons à la recherche fondamentale sur les nouvelles réactions en cascade impliquant l’activation C-H/la carbonylation, les synthèses totales de produits naturels et la chimie des flux.

La chimie des flux est appliquée à la synthèse de produits naturels et à l’optimisation de diverses étapes de réaction lors de la préparation d’une gamme de produits différents.

Les membres de notre groupe de recherche participent activement à la résolution de problèmes de recherche réels, ce qui garantit l’acquisition de connaissances pour les programmes de synthèse/recherche personnalisés de nos clients.

Recent advances in the construction of isoindolo[2,1-a]indol/indolin-6-ones via C-C cross-coupling reactions

Martin Markovič, Peter Koóš, Tomáš Čarný and Tibor GraczaTetrahedron Letters Volume 61, Issue 40Date de publication: 20 August 2020.

The review summaries the most recent synthetic methodologies for assembly of the 6H-isoindolo[2,1-a]indol-6-one and 10b,11-dihydro-6H-isoindolo[2,1-a]indol-6-one scaffolds, the structural motifs present in many natural and biologically interesting compounds. The literature covered in this overview dates from January 2015 to April 2020, and presented strategies are based on transition metal-catalysed C-C cross coupling reactions.

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Recent Applications of Continuous Flow in Homogeneous Palladium Catalysis

Martin Markovič, Pavol Lopatka, Tibor Gracza and Peter KoóšSynthesis 2020; 52(23): 3511-3529Date de publication: Jan 1, 2020

Considerable advances have been made using continuous flow chemistry as an enabling tool in organic synthesis. Consequently, the number of articles reporting continuous flow methods has increased significantly in recent years. This review covers the progress achieved in homogeneous palladium catalysis using continuous flow conditions over the last five years, including C–C/C–N cross-coupling reactions, carbonylations and reductive/oxidative transformations.

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Continuous Pd-Catalyzed Carbonylative Cyclization Using Iron Pentacarbonyl as a CO Source

Pavol Lopatka, Martin Markovič, Peter Koóš, Steven V. Ley and Tibor GraczaJ. Org. Chem. 2019, 84, 22, 14394–14406Date de publication: October 24, 2019

This work discloses a continuous flow carbonylation reaction using iron pentacarbonyl as source of CO. The described transformation using this surrogate was designed for use in commonly accessible flow equipment. Optimized conditions were applied to a scalable synthesis of the natural compound isolated from perianal glandular pheromone secretion of the African civet cat. In addition, a flow Pd-catalyzed carbonylation of aryl halides is successfully reported.

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One-Step Synthesis of Isoindolo[2,1-a]indol-6-ones via Tandem Pd-Catalyzed Aminocarbonylation and C–H Activation

Tomáš Čarný, Martin Markovič, Tibor Gracza and Peter KoóšJ. Org. Chem. 2019, 84, 19, 12499–12507Date de publication: September 11, 2019

A unified catalytic system for tandem Pd-catalyzed carbonylation and C–C cross-coupling via C–H activation was designed. The proposed cascade reaction allows a facile one-step construction of a tetracyclic isoindoloindole skeleton, in which three new C–C/C–N bonds are simultaneously formed. In detail, the carbonylation of aryl dibromides with indoles and C–H activation of in situ formed N-(2’-bromoaroyl)-indole provide biologically relevant 6H-isoindolo[2,1-a]indol-6-ones from commercially available substrates. The aminocarbonylation step in the proposed tandem reaction utilizes glyoxylic acid monohydrate as an environmentally friendly CO surrogate.

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A Short Asymmetric Synthesis of Sauropunols A–D

Martin Markovič, Peter Koóš and Tibor GraczaSynthesis 2017; 49(13): 2939-2942Date de publication: Jan 1, 2017

A short and efficient asymmetric synthesis of natural sauropunols A, B, and C/D has been accomplished in 6 steps from divinylcarbinol with overall yield of 19%, 7% and 32%, respectively. The key synthetic steps include effective Sharpless asymmetric epoxidation of penta-1,4-dien-3-ol and a highly diastereoselective Pd-catalysed oxycarbonylation of pentene-1,2,3-triol. The structures of sauropunols A and B have been confirmed.

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Glyoxylic Acid as a Carbon Monoxide Source for Carbonylation Reactions

Martin Markovič, Pavol Lopatka, Peter Koóš and Tibor GraczaChemistrySelect 2016, 1, 2454-2457Date de publication: 12 July 2016

A new protocol for the generation of carbon monoxide by the dehydration of glyoxylic acid has been developed. Glyoxylic acid was applied as an environmentally friendly and cheap substitute for toxic and gaseous CO in the palladium-catalyzed carbonylation reactions providing industrially interesting products in good to excellent yields.

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Zn-Mediated Reduction of Oxalyl Chloride Forming CO and Its Application in Carbonylation Reactions

Martin Markovič, Pavol Lopatka, Peter Koóš and Tibor GraczaOrg. Lett. 2015, 17, 22, 5618–5621Date de publication: November 10, 2015

An efficient protocol for the generation of carbon monoxide by Zn-mediated reduction of oxalyl chloride has been developed. Oxalyl chloride was applied as an extremely effective substitute for toxic gaseous CO in the palladium-catalyzed alkoxy-/amino-/hydrogen-/hydroxycarbonylation processes providing industrially interesting esters, amides, aldehydes, and carboxylic acids in good to excellent yields. This new procedure can be applied to various carbonylation reactions in the presence of a transition metal catalyst under mild conditions and with a stoichiometric amount of CO source.

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Palladium-catalysed cyclisation of alkenols: Synthesis of oxaheterocycles as core intermediates of natural compounds

Miroslav Palík, Jozef Kožíšek, Peter Koóš and Tibor GraczaBeilstein J. Org. Chem. 2014, 10, 2077–2086.Publication Date: 03 Sep 2014

The study of Pd-catalysed cyclisation reactions of alkenols using different catalytic systems is reported. These transformations affect the stereoselective construction of mono- and/or bicyclic oxaheterocyclic derivatives depending on a starting alkenol. The substrate scope and proposed mechanism of Pd-catalysed cyclisation reactions are also discussed. Moreover, the diastereoselective Pd-catalysed cyclisation of appropriate alkenols to tetrahydrofurans and subsequent cyclisation provided properly substituted 2,5-dioxabicyclo[2.2.1]heptane and 2,6-dioxabicyclo[3.2.1]octane, respectively. Such bicyclic ring subunits are found in many natural products including ocellenynes and aurovertines.

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A General Continuous Flow Method for Palladium Catalysed Carbonylation Reactions Using Single and Multiple Tube-in-Tube Gas-Liquid Microreactors.

Ulrike Gross, Peter Koos, Matthew O’Brien, Anastasios Polyzos and Steven V. LeyEur. J. Org. Chem. 2014, 6418-6430Publication Date: 04 September 2014

A series of continuous flow chemistry processes that facilitate the palladium-catalysed carbonylation of aryl and vinyl iodides and aryl bromides with a range of alkoxy, hydroxy and amino nucleophiles is reported. Harnessing a semipermeable Teflon® AF-2400 Tube-in-Tube assembly, these reactors permit the controlled transport of carbon monoxide into solution at elevated pressure to generate homogeneous flow streams, avoiding some potential issues associated with segmented flow gas-liquid reactors. As the volume of pressurised gas contained within the device is low, the hazards associated with this are potentially mitigated relative to comparable batch processes. We also show how the incorporation of a second in-line gas-flow reactor allows for the sequential introduction of two gases (carbon monoxide and a gaseous nucleophile) into the reaction stream.

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Palladium-catalysed cyclisation of alkenols: Synthesis of oxaheterocycles as core intermediates of natural compounds.

Miroslav Palík, Jozef Kožíšek, Peter Koóš and Tibor GraczaBeilstein J. Org. Chem. 2014, 10, 2077-2086Publication Date: 03 Sep 2014

The study of Pd-catalysed cyclisation reactions of alkenols using different catalytic systems is reported. These transformations affect the stereoselective construction of mono- and/or bicyclic oxaheterocyclic derivatives depending on a starting alkenol. The substrate scope and proposed mechanism of Pd-catalysed cyclisation reactions are also discussed. Moreover, the diastereoselective Pd-catalysed cyclisation of appropriate alkenols to tetrahydrofurans and subsequent cyclisation provided properly substituted 2,5-dioxabicyclo[2.2.1]heptane and 2,6-dioxabicyclo[3.2.1]octane, respectively. Such bicyclic ring subunits are found in many natural products including ocellenynes and aurovertines.

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