MARIA ELISABETTA BRENNA
- Type
- Persona (Classe)
- Label
- MARIA ELISABETTA BRENNA (literal)
- MARIA ELISABETTA BRENNA (literal)
- Persona in rapporto
- Rapporto con CNR di MARIA ELISABETTA BRENNA (Rapporto con CNR)
- Autore CNR di
- Multi-enzyme stereoselective procedures for fragrance chemistry (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Substrate scope and synthetic applications of the enantioselective reduction of ?-alkyl-?-arylenones mediated by Old Yellow Enzymes (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Steric Effects on the Stereochemistry of Old Yellow Enzyme-Mediated Reductions of Unsaturated Diesters: Flipping of the Substrate within the Enzyme Active Site Induced by Structural Modifications (Articolo in rivista) (Prodotto della ricerca)
- Enzymatic-organo-catalysis: metal-free preparation of fragrances by a laccase/ene-reductase/oxa- ammonium catalytic system (Comunicazione a convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1303)
- Biocatalyzed Enantioselective Reduction of Activated C=C Bonds: Synthesis of Enantiomerically Enriched alpha-Halo-beta-arylpropionic Acids (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Enzyme-catalysed apporach to the preparatoin of triazole antifungals: Synthesis of (-)-genaconazole (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Productivity enhancement of C=C bioreductions by coupling by the in situ substrate feedindg product removal technology with isolated enzymes (Abstract/Comunicazione in atti di convegno) (Prodotto della ricerca)
- Biocatalyzed enantioselective reduction of activated C=C bonds: synthesis of enantiomerically enriched alpha-halo-beta-arylprpionic acids (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- Synthesis and olfactory evaluation of all stereoisomers of the fragrance Nectaryl (R) (Articolo in rivista) (Prodotto della ricerca)
- Synthesis of L- and D-4,6-Dideoxyhexoses and 4,6-Dideoxy-C-phenylglycosides from Enzyme-Generated Products (Articolo in rivista) (Prodotto della ricerca)
- Applications of biocatalysis in fragrance chemistry: the enantiomers of alpha-, beta-, and gamma-irones (Articolo in rivista) (Prodotto della ricerca)
- Synthesis, olfactory evaluation and determination of the absolute configuration of the beta- and gamma-Iralia (R) isomers (Articolo in rivista) (Prodotto della ricerca)
- Enantioselective C=C bond reduction of unsaturated alpha-chloro esters by old yellow enzymes (Articolo in rivista) (Prodotto della ricerca)
- Monitoring the synthetic procedures of commercial drugs by H-2 NMR spectroscopy: The case of ibuprofen and naproxen (Articolo in rivista) (Prodotto della ricerca)
- Impurities of tazarotene: Isolation and structural characterisation (Articolo in rivista) (Prodotto della ricerca)
- Biocatalytic methods for the synthesis of enantioenriched odor active compounds (Articolo in rivista) (Prodotto della ricerca)
- Two easy photochemical methods for the conversion of commercial ionone alpha into regioisomerically enriched gamma-ionone and gamma-dihydroionone (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- New synthetic approach to atypical retinoids: application of a versatile annulation procedure (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Cascade coupling of ene-reductases with alcohol dehydrogenases: enantioselective reduction of prochiral unsaturated aldehydes (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Recent advances in the benzannulation of substituted 3-alkoxycarbonyl-3,5-hexadienoic acids and 3-alkoxycarbonylhex-3-en-5-ynoic acids to polysubstituted aromatics (Articolo in rivista) (Prodotto della ricerca)
- The enantiomers of Iralia (R): preparation and odour evaluation (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Establishing the synthetic origin of illicit drugs by 2H NMR spectroscopy (Comunicazione a convegno) (Prodotto della ricerca)
- On the stereochemistry of the Baker's Yeast-mediated reduction of regioisomeric unsaturated aldehydes: Examples of enantioselectivity switch promoted by substrate-engineering (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Traceability of synthetic drugs by position-specific deuterium isotope ratio analysis - The case of Prozac and the fluoxetine generics (Articolo in rivista) (Prodotto della ricerca)
- Isolation and characterisation of a phenolic impurity in a commercial sample of duloxetine (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Lipase-catalysed synthesis of homotartaric acid enantiomers (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Isolation and characterisation of impurities in adapalene (Articolo in rivista) (Prodotto della ricerca)
- Synthesis, olfactory evaluation, determination of the absolute configuration of the 3,4-dehydroionone stereoisomers (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Coautore
- DANIELA MONTI (Persona)
- GIOVANNI FRONZA (Unità di personale esterno)
- STEFANO SERRA (Unità di personale interno)
- GIOVANNI FRONZA (Persona)
- CLAUDIO FUGANTI (Unità di personale esterno)
- ERICA ELISA FERRANDI (Persona)
- Nome
- MARIA ELISABETTA (literal)
- Cognome
- BRENNA (literal)
- Afferisce a
- Ha pubblicazioni con
- GIOVANNI FRONZA (Persona)
- CLAUDIO FUGANTI (Unità di personale esterno)
- STEFANO SERRA (Unità di personale interno)
Incoming links:
- Coautore
- GIOVANNI FRONZA (Persona)
- STEFANO SERRA (Unità di personale interno)
- DANIELA MONTI (Persona)
- ERICA ELISA FERRANDI (Persona)
- CLAUDIO FUGANTI (Unità di personale esterno)
- GIOVANNI FRONZA (Unità di personale esterno)
- Ha pubblicazioni con
- GIOVANNI FRONZA (Persona)
- STEFANO SERRA (Unità di personale interno)
- CLAUDIO FUGANTI (Unità di personale esterno)
- Ha afferente
- Rapporto con persona
- Rapporto con CNR di MARIA ELISABETTA BRENNA (Rapporto con CNR)
- Autore CNR
- New synthetic approach to atypical retinoids: application of a versatile annulation procedure (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Synthesis, olfactory evaluation and determination of the absolute configuration of the beta- and gamma-Iralia (R) isomers (Articolo in rivista) (Prodotto della ricerca)
- Synthesis of L- and D-4,6-Dideoxyhexoses and 4,6-Dideoxy-C-phenylglycosides from Enzyme-Generated Products (Articolo in rivista) (Prodotto della ricerca)
- Applications of biocatalysis in fragrance chemistry: the enantiomers of alpha-, beta-, and gamma-irones (Articolo in rivista) (Prodotto della ricerca)
- Synthesis and olfactory evaluation of all stereoisomers of the fragrance Nectaryl (R) (Articolo in rivista) (Prodotto della ricerca)
- Lipase-catalysed synthesis of homotartaric acid enantiomers (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Enantioselective C=C bond reduction of unsaturated alpha-chloro esters by old yellow enzymes (Articolo in rivista) (Prodotto della ricerca)
- Isolation and characterisation of a phenolic impurity in a commercial sample of duloxetine (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- The enantiomers of Iralia (R): preparation and odour evaluation (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Recent advances in the benzannulation of substituted 3-alkoxycarbonyl-3,5-hexadienoic acids and 3-alkoxycarbonylhex-3-en-5-ynoic acids to polysubstituted aromatics (Articolo in rivista) (Prodotto della ricerca)
- Two easy photochemical methods for the conversion of commercial ionone alpha into regioisomerically enriched gamma-ionone and gamma-dihydroionone (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Monitoring the synthetic procedures of commercial drugs by H-2 NMR spectroscopy: The case of ibuprofen and naproxen (Articolo in rivista) (Prodotto della ricerca)
- Impurities of tazarotene: Isolation and structural characterisation (Articolo in rivista) (Prodotto della ricerca)
- Biocatalytic methods for the synthesis of enantioenriched odor active compounds (Articolo in rivista) (Prodotto della ricerca)
- Isolation and characterisation of impurities in adapalene (Articolo in rivista) (Prodotto della ricerca)
- Traceability of synthetic drugs by position-specific deuterium isotope ratio analysis - The case of Prozac and the fluoxetine generics (Articolo in rivista) (Prodotto della ricerca)
- Enzyme-catalysed apporach to the preparatoin of triazole antifungals: Synthesis of (-)-genaconazole (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Biocatalyzed Enantioselective Reduction of Activated C=C Bonds: Synthesis of Enantiomerically Enriched alpha-Halo-beta-arylpropionic Acids (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Synthesis, olfactory evaluation, determination of the absolute configuration of the 3,4-dehydroionone stereoisomers (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Establishing the synthetic origin of illicit drugs by 2H NMR spectroscopy (Comunicazione a convegno) (Prodotto della ricerca)
- Steric Effects on the Stereochemistry of Old Yellow Enzyme-Mediated Reductions of Unsaturated Diesters: Flipping of the Substrate within the Enzyme Active Site Induced by Structural Modifications (Articolo in rivista) (Prodotto della ricerca)
- Biocatalyzed enantioselective reduction of activated C=C bonds: synthesis of enantiomerically enriched alpha-halo-beta-arylprpionic acids (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
- On the stereochemistry of the Baker's Yeast-mediated reduction of regioisomeric unsaturated aldehydes: Examples of enantioselectivity switch promoted by substrate-engineering (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Cascade coupling of ene-reductases with alcohol dehydrogenases: enantioselective reduction of prochiral unsaturated aldehydes (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Productivity enhancement of C=C bioreductions by coupling by the in situ substrate feedindg product removal technology with isolated enzymes (Abstract/Comunicazione in atti di convegno) (Prodotto della ricerca)
- Enzymatic-organo-catalysis: metal-free preparation of fragrances by a laccase/ene-reductase/oxa- ammonium catalytic system (Comunicazione a convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1303)
- Substrate scope and synthetic applications of the enantioselective reduction of ?-alkyl-?-arylenones mediated by Old Yellow Enzymes (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Multi-enzyme stereoselective procedures for fragrance chemistry (Abstract/Poster in atti di convegno) (Prodotto della ricerca)