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المؤلفون: Riccardo Riccioli, Vasco Corti, Ada Martinelli, Mariafrancesca Fochi, Luca Bernardi, Sofia Sandri
المساهمون: Corti V., Riccioli R., Martinelli A., Sandri S., Fochi M., Bernardi L.
المصدر: Chemical Science
مصطلحات موضوعية: chemistry.chemical_classification, Trifluoromethyl, Stereodivergency, 010405 organic chemistry, Stereochemistry, Chemistry, General Chemistry, 010402 general chemistry, Ring (chemistry), 01 natural sciences, 0104 chemical sciences, Catalysis, Amino acid, Transfer Hydrogenation, chemistry.chemical_compound, Organocatalysi, Asymmetric Synthesi, Chirality (chemistry)
وصف الملف: ELETTRONICO
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98287a03357ab73ca89ae654c4b63500
http://europepmc.org/articles/PMC8336586 -
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المؤلفون: Carmen Festa, Veronica Esposito, Daniela Benigno, Simona De Marino, Angela Zampella, Antonella Virgilio, Aldo Galeone
المساهمون: Festa, Carmen, Esposito, Veronica, Benigno, Daniela, DE MARINO, Simona, Zampella, Angela, Virgilio, Antonella, Galeone, Aldo
المصدر: International Journal of Molecular Sciences; Volume 23; Issue 3; Pages: 1092
International Journal of Molecular Sciences, Vol 23, Iss 1092, p 1092 (2022)مصطلحات موضوعية: QH301-705.5, asymmetric synthesis, Oligonucleotides, Catalysis, Sulfoxidation, Inorganic Chemistry, Humans, heterocyclic compounds, Catalytic DNA, Biology (General), Physical and Theoretical Chemistry, Asymmetric synthesi, QD1-999, Molecular Biology, Spectroscopy, Deoxyadenosines, Organic Chemistry, Stereoisomerism, General Medicine, DNA, Telomere, Computer Science Applications, Telomeric G-quadruplex analogues, G-Quadruplexes, Chemistry, catalytic DNA, telomeric G-quadruplex analogues, sulfoxidation
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1555748f8ac225d14c7f6e9a43253b48
http://hdl.handle.net/11588/870274 -
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المؤلفون: Luca Bernardi, Armando Carlone, Francesco Fini
المساهمون: Bernardi, L., Ricci, A., Carlone, A., Fini, F.
المصدر: Methodologies in Amine Synthesis
مصطلحات موضوعية: Active ingredient, Organocatalysi, Chemistry, Organocatalysis, Scale-up, Enantioselective synthesis, Active Pharmaceutical Ingredient, Amine gas treating, Asymmetric synthesi, Industrialization, Chirality (chemistry), Combinatorial chemistry, Chiral amine
وصف الملف: STAMPA
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8744191fb78872dfa2389bd1ea8415eb
http://hdl.handle.net/11585/852140 -
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المؤلفون: Mariafrancesca Fochi, Luca Bernardi, Giulio Bertuzzi, Daniel Pecorari, Andrea Mazzanti, Filippo Silvestrini, Pierluigi Moimare
المساهمون: Bertuzzi G., Silvestrini F., Moimare P., Pecorari D., Mazzanti A., Bernardi L., Fochi M.
مصطلحات موضوعية: Chemistry, Phase (matter), Heterocycle, Asymmetric Synthesi, Michael reaction, Enantioselective synthesis, General Chemistry, Cascade Reaction, Combinatorial chemistry, Sulfa-Michael addition, Catalysis, Phase-Transfer Catalysi
وصف الملف: ELETTRONICO
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab4ca1632e58d80698c190a6934fce7b
https://hdl.handle.net/11585/787177 -
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المؤلفون: Claudio Curti, Marco Lombardo, Andrea Sartori, Vincenzo Zambrano, Lucia Battistini, Franca Zanardi, Gloria Rassu, Luigi Pinna, Giorgio Pelosi
المساهمون: Curti C., Rassu G., Lombardo M., Zambrano V., Pinna L., Battistini L., Sartori A., Pelosi G., Zanardi F.
مصطلحات موضوعية: chemistry.chemical_classification, Bicyclic molecule, 010405 organic chemistry, Enantioselective synthesis, asymmetric synthesi, Vinylogy, Iminium, General Medicine, General Chemistry, 010402 general chemistry, 01 natural sciences, Combinatorial chemistry, Aldehyde, Catalysis, Cycloaddition, 0104 chemical sciences, fused-ring system, Enantiopure drug, chemistry, Organocatalysis, organocatalysis, cycloaddition, heterocycle
وصف الملف: STAMPA
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ef54f4cd3cc34aa92c75ddf27dfacc5
https://hdl.handle.net/11585/778320 -
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المؤلفون: Aguilera D. A., Tanchoux N., Fochi M., Bernardi L.
المساهمون: Aguilera D.A., Tanchoux N., Fochi M., Bernardi L.
مصطلحات موضوعية: Chitosan, Heterogeneous catalysi, Renewable resources, Alginate, Asymmetric synthesi
وصف الملف: ELETTRONICO
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______4094::c1fe637ddaef94c338a1b8ad9c3b4d22
https://hdl.handle.net/11585/787163 -
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المؤلفون: Giovanni N. Roviello, Hayarpi M. Simonyan, Ashot S. Saghyan, Rosanna Palumbo, Agnieszka Belter, Anna F. Mkrtchyan, Marta A. Fik-Jaskółka, Valentina Roviello, Liana A. Hayriyan
المساهمون: Fik-Jaskolka, M. A., Mkrtchyan, A. F., Saghyan, A. S., Palumbo, R., Belter, A., Hayriyan, L. A., Simonyan, H., Roviello, V., Roviello, G. N.
مصطلحات موضوعية: 0301 basic medicine, Circular dichroism, BSA, Stereochemistry, Phenylalanine, Clinical Biochemistry, Alkyne, Antineoplastic Agents, Antiparallel (biochemistry), Biochemistry, 03 medical and health sciences, Quadruplex DNA, Neoplasms, Copper binding, Moiety, Humans, Bovine serum albumin, Asymmetric synthesi, Protein secondary structure, Cell Proliferation, chemistry.chemical_classification, Binding Sites, 030102 biochemistry & molecular biology, biology, Chemistry, Organic Chemistry, Biological macromolecule, Serum Albumin, Bovine, Molecular Docking Simulation, 030104 developmental biology, Alkynes, Nickel complexe, Molecular docking, biology.protein, Copper, Macromolecule, Protein Binding
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da05ca69e9456fc01596fc080c809efe
http://hdl.handle.net/11588/818951 -
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المؤلفون: Giorgio Della Sala, Rafael Cano, Vito Capaccio, Marina Sicignano, José Alemán, Luca Bernardi, Francesco De Riccardis, Sergio Díaz-Tendero, Ricardo I. Rodríguez, Fabio Borello
المساهمون: UAM. Departamento de Química, UAM. Departamento de Química Orgánica, Sicignano M., Rodriguez R.I., Capaccio V., Borello F., Cano R., De Riccardis F., Bernardi L., Diaz-Tendero S., Della Sala G., Aleman J.
المصدر: Biblos-e Archivo: Repositorio Institucional de la UAM
Universidad Autónoma de Madrid
Biblos-e Archivo. Repositorio Institucional de la UAM
instnameمصطلحات موضوعية: Chemistry, Organic Chemistry, Enantioselective synthesis, Quinidinium, Chiral phase, Química, Azlactone, Biochemistry, Electron, Catalysis, Phase-Transfer Catalysi, Transfer (group theory), Computational chemistry, Phase (matter), Trifluormethylthiolation, Asymmetric synthesi, Physical and Theoretical Chemistry, Aryl groups
وصف الملف: application/pdf; ELETTRONICO
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55268c1099b9ac32196dcf673acfc111
http://hdl.handle.net/10486/690789 -
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المؤلفون: Stefano Superchi, Francesca Casella, Giulia Marsico, Marco Masi, Jun-Hyung Tak, Antonio Evidente, Jeffrey R. Bloomquist, Patrizia Scafato, Barbara A. Pignataro, Maria Chiara Zonno
المساهمون: Marsico, Giulia, Pignataro, Barbara A., Masi, Marco, Evidente, Antonio, Casella, Francesca, Zonno, Maria Chiara, Tak, Jun-Hyung, Bloomquist, Jeffrey R., Superchi, Stefano, Scafato, Patrizia
المصدر: Tetrahedron. 74:3912-3923
مصطلحات موضوعية: Coupling reaction, Colletochlorin A, 010405 organic chemistry, Chemistry, Drug Discovery3003 Pharmaceutical Science, Organic Chemistry, Enantioselective synthesis, Absolute configuration, Total synthesis, 010402 general chemistry, Colletorin A, 01 natural sciences, Biochemistry, Combinatorial chemistry, 0104 chemical sciences, Turn (biochemistry), Bioactive fungal metabolite, Drug Discovery, Halogen, Asymmetric synthesi, Enantiomer, Sharpless asymmetric dihydroxylation, Asymmetric dihydroxylation
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المؤلفون: Aguilera D. A., Spinozzi Di Sante L., Pettignano A., Riccioli R., Roeske J., Albergati L., Corti V., Fochi M., Bernardi L., Quignard F., Tanchoux N.
المساهمون: Aguilera D.A., Spinozzi Di Sante L., Pettignano A., Riccioli R., Roeske J., Albergati L., Corti V., Fochi M., Bernardi L., Quignard F., Tanchoux N.
مصطلحات موضوعية: Heterogeneous catalysi, Organocatalysi, Renewable resources, Alginate, Asymmetric synthesi
وصف الملف: ELETTRONICO
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______4094::dd27acb769bb6849b398536de0f6611c
http://hdl.handle.net/11585/725135