المؤلفون: Ivan Bassanini, Simone Grosso, Chiara Tognoli, Giovanni Fronza, Sergio Riva

المصدر: International Journal of Molecular Sciences, Vol 24, Iss 4, p 3524 (2023)

مصطلحات موضوعية: biocatalyzed [2 + 2] olefin cycloaddition, T. versicolor laccases, anilines, bio-oxidation, radical chemistry, Biology (General), QH301-705.5, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1422-0067/24/4/3524; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067

URL الوصول: https://doaj.org/article/aebd94e9b3104f3997ec796dfbe734ac

المؤلفون: Giovanni Fronza, Claudio Fuganti, Piero Grasselli, Stefano Servi

المصدر: CHIMIA, Vol 47, Iss 4 (1993)

مصطلحات موضوعية: Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://chimia.ch/chimia/article/view/2223; https://doaj.org/toc/0009-4293; https://doaj.org/toc/2673-2424

URL الوصول: https://doaj.org/article/8afdac38f4884a0c94061014b7f40f24

المؤلفون: Erica Elisa Ferrandi, Ivan Bassanini, Giovanni Fronza, Sergio Riva, Daniela Monti, Susanna Bertuletti

المصدر: ChemCatChem
(2021). doi:10.1002/cctc.202101307
info:cnr-pdr/source/autori:Bertuletti S.; Ferrandi E.E.; Monti D.; Fronza G.; Bassanini I.; Riva S./titolo:Synthesis of ?-Muricholic Acid by One-Pot Enzymatic Mitsunobu Inversion using Hydroxysteroid Dehydrogenases/doi:10.1002%2Fcctc.202101307/rivista:ChemCatChem (Print)/anno:2021/pagina_da:/pagina_a:/intervallo_pagine:/volume

مصطلحات موضوعية: chemistry.chemical_classification, Stereochemistry, Organic Chemistry, Muricholic acid, Hyocholic acid, Hydroxysteroid Dehydrogenases, Inversion (discrete mathematics), Catalysis, Inorganic Chemistry, hyocholic acid · ?-muricholic acid · epimerization ·one-pot reaction · hydroxysteroid dehydrogenases, chemistry.chemical_compound, Enzyme, chemistry, One pot reaction, Epimer, Physical and Theoretical Chemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f591d3b4a4c9179cf3f06f4b0d620a0
https://doi.org/10.1002/cctc.202101307

المؤلفون: Simone Grosso, Fabio Radaelli, Daniela Monti, Giovanni Fronza, Daniele Passarella, Sergio Riva

المصدر: Advanced Synthesis & Catalysis.

مصطلحات موضوعية: Laccase, Chemistry, Organic chemistry, General Chemistry, Catalysis

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::53e0a2d4210eea99cf6c03b6e5377446
https://doi.org/10.1002/adsc.201900190

المؤلفون: Sergio Riva, Federica Bertacchi, Paolo Gavezzotti, Daniela Monti, Vladimír Křen, Giovanni Fronza

المصدر: Advanced synthesis & catalysis
357 (2015): 1831–1839. doi:10.1002/adsc.201500185
info:cnr-pdr/source/autori:Gavezzotti, Paolo; Bertacchi, Federica; Fronza, Giovanni; Kren, Vladimir; Monti, Daniela; Riva, Sergio/titolo:Laccase-Catalyzed Dimerization of Piceid, a Resveratrol Glucoside, and its Further Enzymatic Elaboration/doi:10.1002%2Fadsc.201500185/rivista:Advanced synthesis & catalysis (Print)/anno:2015/pagina_da:1831/pagina_a:1839/intervallo_pagine:1831–1839/volume:357

مصطلحات موضوعية: viniferin, chemistry.chemical_classification, Laccase, Viniferin, General Chemistry, resveratrol, Resveratrol, laccase, Catalysis, chemistry.chemical_compound, Enzyme, piceid, chemistry, Glucoside, glycosidase, Organic chemistry, Glycoside hydrolase, Piceid

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::955d347063ae6f6ba79e8ad1cae25715
https://doi.org/10.1002/adsc.201500185

المؤلفون: Paolo Ronchi, Elisabetta Brenna, Alessia Manfredi, Fabio Parmeggiani, Francesco G. Gatti, Giovanni Fronza, Claudio Fuganti

المصدر: Journal of molecular catalysis. B, Enzymatic
84 (2012): 94–101. doi:10.1016/j.molcatb.2012.02.003
info:cnr-pdr/source/autori:Brenna, Elisabetta; Fronza, Giovanni; Fuganti, Claudio; Gatti, Francesco G.; Manfredi, Alessia; Parmeggiani, Fabio; Ronchi, Paolo/titolo:On the stereochemistry of the Baker's Yeast-mediated reduction of regioisomeric unsaturated aldehydes: Examples of enantioselectivity switch promoted by substrate-engineering/doi:10.1016%2Fj.molcatb.2012.02.003/rivista:Journal of molecular catalysis. B, Enzymatic (Print)/anno:2012/pagina_da:94/pagina_a:101/intervallo_pagine:94–101/volume:84

مصطلحات موضوعية: Deuterium NMR spectroscopy, Unsaturated aldehydes, Chemistry, Stereochemistry, Process Chemistry and Technology, Enantioselective synthesis, Substrate (chemistry), Bioengineering, Enantioselectivity, Biochemistry, Catalysis, Yeast, Labelling, Structural isomer, Baker's Yeast, Organic chemistry, Fermentation, Enantiomer, Enantiomeric excess, Reduction

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1645a2a159aabde0a250acffec37f4fa
https://doi.org/10.1016/j.molcatb.2012.02.003

المؤلفون: Giovanni Fronza, Gianluca Nasini, Adriana Bava

المصدر: Journal of molecular catalysis. B, Enzymatic
82 (2012): 59–63. doi:10.1016/j.molcatb.2012.06.006
info:cnr-pdr/source/autori:Bava, Adriana; Nasini, Gianluca; Fronza, Giovanni/titolo:Biotransformation of spirolaxine by Absidia cuneospora and Trametes hirsuta: Formation of beta-glycosyl and beta-xylosyl derivatives/doi:10.1016%2Fj.molcatb.2012.06.006/rivista:Journal of molecular catalysis. B, Enzymatic (Print)/anno:2012/pagina_da:59/pagina_a:63/intervallo_pagine:59–63/volume:82

مصطلحات موضوعية: biology, Semi-synthesis, Stereochemistry, Process Chemistry and Technology, Metabolite, Absidia cuneospora, Bioengineering, Trametes hirsuta, biology.organism_classification, Biochemistry, Nmr data, Catalysis, Glycosyl and xylosyl derivative, chemistry.chemical_compound, Hydrolysis, chemistry, Biotransformation, Fungal metabolites, Organic chemistry, Glycosyl, Spirolaxine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6234cb5e5a64cebeea0c42f952fcdf1d
https://doi.org/10.1016/j.molcatb.2012.06.006

المؤلفون: Stefano Serra, Giovanni Fronza

المصدر: European journal of organic chemistry
(2012): 4838–4843. doi:10.1002/ejoc.201200620
info:cnr-pdr/source/autori:Serra, Stefano; Fronza, Giovanni/titolo:Unambiguous Characterization of the Sesquiterpene (7R,9E)-1,2,11-Trihydroxy-1,3,5,9-bisabolatetraene through Its Enantioselective Synthesis/doi:10.1002%2Fejoc.201200620/rivista:European journal of organic chemistry (Print)/anno:2012/pagina_da:4838/pagina_a:4843/intervallo_pagine:4838–4843/volume

مصطلحات موضوعية: Natural products, Configuration determination, Natural product, Stereochemistry, Terpenoids, Chemical structure, Organic Chemistry, Enantioselective synthesis, Absolute configuration, Sesquiterpene, Chiral resolution, Enzymes, chemistry.chemical_compound, chemistry, Chromane, Organic chemistry, Chemical stability, Physical and Theoretical Chemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32db659be7a2632a14cd4e1983019730
https://doi.org/10.1002/ejoc.201200620

المؤلفون: Gianluca Nasini, Giovanni Fronza, Alberto Arnone, Adriana Bava

المصدر: Journal of Natural Products. 72:2000-2004

مصطلحات موضوعية: Bridged-Ring Compounds, Double bond, Stereochemistry, Pharmaceutical Science, Ring (chemistry), Oxetane, Analytical Chemistry, Structure-Activity Relationship, chemistry.chemical_compound, Transacylation, Ascomycota, Ethers, Cyclic, Drug Discovery, Biotransformation, Bond cleavage, Pharmacology, chemistry.chemical_classification, Molecular Structure, Organic Chemistry, Stereoisomerism, Complementary and alternative medicine, chemistry, Molecular Medicine, Hemiacetal, Taxoids, Epimer, Diterpene

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::736c33df764654943d30e1d2c7ac5049
https://doi.org/10.1021/np900368u

المؤلفون: Daniela Acetti, Claudio Fuganti, Elisabetta Brenna, Giovanni Fronza

المصدر: Talanta. 76:651-655

مصطلحات موضوعية: Naproxen, Magnetic Resonance Spectroscopy, Chemistry, education, Analytical chemistry, Ibuprofen, Nuclear magnetic resonance spectroscopy, Deuterium, Isotopic composition, Analytical Chemistry, Pharmaceutical Preparations, medicine, Proton NMR, Spectroscopy, Nuclear chemistry, medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1619f9b172273ab025489f2109576df6
https://doi.org/10.1016/j.talanta.2008.04.009