المؤلفون: Antonia Di Mola, Giorgia Nicastro, Lorenzo Serusi, Rosanna Filosa, Mario Waser, Antonio Massa

المصدر: Molecules, Vol 27, Iss 17, p 5647 (2022)

مصطلحات موضوعية: heterocycles, asymmetric synthesis, isoindolinones, Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1420-3049/27/17/5647; https://doaj.org/toc/1420-3049

URL الوصول: https://doaj.org/article/802ecc4f35f940bca7806956c4b6e46e

المؤلفون: Antonia Di Mola, Felice De Piano, Lorenzo Serusi, Giovanni Pierri, Laura Palombi, Antonio Massa

المصدر: International Journal of Molecular Sciences; Volume 24; Issue 6; Pages: 5783

مصطلحات موضوعية: heterocycles, organocatalysis, asymmetric synthesis, hybrid molecules

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Physical Chemistry and Chemical Physics; https://dx.doi.org/10.3390/ijms24065783

الاتاحة: https://doi.org/10.3390/ijms24065783

المؤلفون: Lorenzo Serusi (6112487), Antonio Massa (588938), Consiglia Tedesco (1748401), Amedeo Capobianco (734860), Laura Palombi (731436)

مصطلحات موضوعية: Biophysics, Biochemistry, Microbiology, Molecular Biology, Biotechnology, Evolutionary Biology, Ecology, Sociology, Infectious Diseases, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, 2- carbobenzyloxy, rationale, Sulfur Stereocenters, tosylbenzylidenimine, organocatalytic, 3- sulfinyl-substituted isoindolinones, oxidation reaction, diastereocontrol, acetal, sulfoxidation, transformation, DFT calculations, enantioenriched isoindolinone N, Sulfinyl-Substituted, tandem, stereoselectivity, stereoselective access, Enantioselective Synthesis, First

Relation: https://figshare.com/articles/journal_contribution/The_First_Highly_Enantioselective_Synthesis_of_3_Sulfinyl-Substituted_Isoindolinones_Having_Adjacent_Carbon_and_Sulfur_Stereocenters/14977425

الاتاحة: https://doi.org/10.1021/acs.joc.1c01300.s001

المؤلفون: Lorenzo Serusi, Antonia Di Mola, Antonio Massa

المصدر: RSC Advances. 13:6557-6563

مصطلحات موضوعية: General Chemical Engineering, General Chemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f34f9718e2a82977c3795731c8712b0f
https://doi.org/10.1039/d3ra00378g

المؤلفون: Lorenzo Serusi, Paul Zebrowski, Johannes Schörgenhumer, Antonio Massa, Mario Waser

المصدر: Helvetica Chimica Acta. 105

مصطلحات موضوعية: Inorganic Chemistry, amino acids, cascade reactions, cyclization, heterocycles, organocatalysis, Organic Chemistry, Drug Discovery, Physical and Theoretical Chemistry, Biochemistry, Catalysis

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::294080961f197ab6dd2a934975b713e2
https://doi.org/10.1002/hlca.202200110

المؤلفون: Angelo Frongia, Francesco Soddu, Giuseppe Peretti, Alberto Luridiana, Federico Cuccu, Lorenzo Serusi, David J. Aitken, Francesco Secci, Pierluigi Caboni

المصدر: Advanced Synthesis & Catalysis. 362:4159-4163

مصطلحات موضوعية: chemistry.chemical_compound, chemistry, Aryl, General Chemistry, Medicinal chemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::8419fced168b8eb4cdce733f6981b471
https://doi.org/10.1002/adsc.202000541

المؤلفون: Lorenzo Serusi, Laura Palombi, Giovanni Pierri, Antonia Di Mola, Antonio Massa

المساهمون: Serusi, Lorenzo, Palombi, Laura, Pierri, Giovanni, DI MOLA, Antonia, Massa, Antonio

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000821394500001; volume:87; firstpage:8420; lastpage:8428; numberofpages:9; journal:JOURNAL OF ORGANIC CHEMISTRY; http://hdl.handle.net/11386/4797269; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85134828467

الاتاحة: http://hdl.handle.net/11386/4797269
https://doi.org/10.1021/acs.joc.2c00518

المؤلفون: David J. Aitken, Angelo Frongia, Pierluigi Caboni, Alberto Luridiana, Francesco Secci, Lorenzo Serusi, Federico Cuccu

المصدر: Organic Letters. 21:7755-7758

مصطلحات موضوعية: Cyclobutanes, Tandem, 010405 organic chemistry, Organic Chemistry, 010402 general chemistry, 01 natural sciences, Biochemistry, 0104 chemical sciences, chemistry.chemical_compound, chemistry, Cascade reaction, Polymer chemistry, Wittig reaction, Phosphonium, Physical and Theoretical Chemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a57402b7c8cace8ad4198f592ed2a2a
https://doi.org/10.1021/acs.orglett.9b02690

المؤلفون: Marie Bonnans, Pierluigi Caboni, Francesco Secci, Lorenzo Serusi, Angelo Frongia, David J. Aitken, Thomas Boddaert, Alberto Luridiana

المصدر: Advanced Synthesis & Catalysis. 361:1908-1912

مصطلحات موضوعية: Thesaurus (information retrieval), Cascade reaction, Chemistry, Organic chemistry, General Chemistry, Brønsted–Lowry acid–base theory, Catalysis

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::621456ade9d77da04b0fe09e6d5154f2
https://doi.org/10.1002/adsc.201900175

المؤلفون: Amedeo Capobianco, Antonio Massa, Consiglia Tedesco, Laura Palombi, Lorenzo Serusi

مصطلحات موضوعية: Tandem, Organic Chemistry, Enantioselective synthesis, sulfoxides, chemistry.chemical_element, Organocatalysts, Combinatorial chemistry, Sulfur, Redox, Stereocenter, chemistry.chemical_compound, Dynamic kinetic asymmetric transformations, Sulphur, Thiourea, chemistry, Stereoselectivity, Bifunctional

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5718aa894122c2ad9dd3f606ec885a84
http://hdl.handle.net/11697/171772

المؤلفون: Benedetta Fois, Laura Škarnulytė, Marco Gaspari, A. Arridu, Ugnė Endriulaitytė, Miglė Paškevičiu̅tė, Elias Maccioni, Simona Distinto, Vilma Petrikaite, Filippo Cottiglia, Rossella Angius, Serenella Deplano, Rita Meleddu, Domenico Taverna, Lorenzo Serusi

المصدر: ACS medicinal chemistry letters. 10(4)

مصطلحات موضوعية: Antitumor activity, Programmed cell death, 010405 organic chemistry, Stereochemistry, Isatin, Organic Chemistry, Substituent, 01 natural sciences, Biochemistry, Chemical synthesis, 0104 chemical sciences, 010404 medicinal & biomolecular chemistry, chemistry.chemical_compound, medicine.anatomical_structure, chemistry, Drug Discovery, medicine, Moiety, Nucleus, EC50

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c72ffa5ba2141e0524250ea3e561a6c6
https://pubmed.ncbi.nlm.nih.gov/30996798