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Profil bibliographique

Chimène Asta

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

8Publications signalées
179Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Enzyme-mediated dye degradationOxidative Organic Chemistry ReactionsEnzyme Catalysis and ImmobilizationCatalysis for Biomass ConversionCyclopropane Reaction Mechanisms

Les publications récentes

2013 article OpenAlex

ChemInform Abstract: Combination of Enzyme‐ and Lewis Acid‐Catalyzed Reactions: A New Method for the Synthesis of 6,7‐Dihydrobenzofuran‐4(5H)‐ones Starting from 2,5‐Dimethylfuran and 1,3‐Cyclohexanediones.

Chimène Asta, D. Schmidt, Juergen Conrad, Wolfgang U. Frey et autres

Abstract The (Z)‐hexenedione (I), previously obtained by laccase‐promoted cleavage of 2,5‐dimethylfuran undergoes Gd‐catalyzed reaction with diones (II) to form dihydrobenzofurans (III).

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0 citations ChemInform
2013 article OpenAlex

The first enzymatic Achmatowicz reaction: selective laccase-catalyzed synthesis of 6-hydroxy-(2H)-pyran-3(6H)-ones and (2H)-pyran-2,5(6H)-diones

Chimène Asta, D. Schmidt, Jürgen Conrad, Bernhard Förster-Fromme et autres

The laccase-catalyzed oxidation of (5-alkylfuran-2-yl)carbinols using aerial oxygen as an oxidant selectively affords 6-hydroxy-(2H)-pyran-3(6H)-ones with yields up to 90%. With suitable substituted furan-2-yl carbinols as substrates the procedure allows the efficient preparation of (2H)-pyran-2,5(6H)-diones in a single step.

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36 citations RSC Advances
2013 article OpenAlex

Combination of enzyme- and Lewis acid-catalyzed reactions: a new method for the synthesis of 6,7-dihydrobenzofuran-4(5H)-ones starting from 2,5-dimethylfuran and 1,3-cyclohexanediones

Chimène Asta, D. Schmidt, Jürgen Conrad, Wolfgang U. Frey et autres

The Lewis acid-catalyzed domino 1,2-addition/1,4-addition/elimination between (Z)-3-hexene-2,5-dione and 1,3-dicarbonyls delivers 3-methyl-6,7-dihydrobenzofuran-4(5H)-ones exclusively with yields up to 82%. The combination of this new process with the laccase-catalyzed formation of (Z)-3-hexene-2,5-dione by oxidative cleavage of 2,5-dimethylfuran allows for the synthesis of 6,7-dihydrobenzofuran-4(5H)-ones starting directly …

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10 citations Organic & Biomolecular Chemistry
Accès ouvert 2013 dataset OpenAlex

CCDC 926712: Experimental Crystal Structure Determination

Chimène Asta, D. Schmidt, Jürgen Conrad, Wolfgang Frey et autres

An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, …

0 citations The Cambridge Structural Database
Accès ouvert 2013 dataset OpenAlex

CCDC 926713: Experimental Crystal Structure Determination

Chimène Asta, D. Schmidt, Jürgen Conrad, Wolfgang Frey et autres

An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, …

0 citations The Cambridge Structural Database
2011 article OpenAlex

Laccase-catalyzed stereoselective oxidative ring opening of 2,5-dialkylfurans into 2-ene-1,4-diones using air as an oxidant

Chimène Asta, Jürgen Conrad, Sabine Mika, Uwe Beifuß

The laccase-catalyzed ring opening of 2,5-dimethylfuran using air as an oxidant stereoselectively yields (Z)- or (E)-3-hexene-2,5-dione depending on the mediator employed: with TEMPO the (Z)-3-hexene-2,5-dione is formed, while a combination of TEMPO and violuric acid gives (E)-3-hexene-2,5-dione. The (Z)-selective ring cleavage was …

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32 citations Green Chemistry

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