نتائج البحث - "Lorenza Ghisu"

1

Sulphide as a leaving group: highly stereoselective bromination of alkyl phenyl sulphides

المؤلفون: John E. O'Brien, Caterina Cioffi, Lorenza Ghisu, Manuel Ruether, Ilaria Biancofiore, Daniele Canestrari, Stefano Lancianesi, Mauro F. A. Adamo, Hasim Ibrahim

المصدر: Chemical Science
Canestrari, Daniele ORCID: 0000-0002-3245-6630 <https://orcid.org/0000-0002-3245-6630>, Cioffi, Caterina, Biancofiore, Ilaria, Lancianesi, Stefano, Ghisu, Lorenza, Ruether, Manuel, O'Brien, John, Adamo, Mauro F.A. ORCID: 0000-0001-9072-3648 <https://orcid.org/0000-0001-9072-3648> and Ibrahim, Hasim ORCID: 0000-0003-1386-3641 <https://orcid.org/0000-0003-1386-3641> (2019) Sulphide as a leaving group: highly stereoselective bromination of alkyl phenyl sulphides. Chemical Science, 10 (39). ISSN 2041-6520

مصطلحات موضوعية: chemistry.chemical_classification, Nitrile, 010405 organic chemistry, Leaving group, Halogenation, Alcohol, General Chemistry, 010402 general chemistry, 01 natural sciences, Medicinal chemistry, 0104 chemical sciences, Adduct, chemistry.chemical_compound, chemistry, Nucleophilic substitution, Stereoselectivity, Alkyl

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c10ef6e83d3dad3ccf2136d457ca2fc5
https://doi.org/10.1039/c9sc03560e

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2

Synthesis of quaternary α-benzyl- and α-allyl-α-methylamino cyclobutanones

المؤلفون: Francesco Secci, Pierluigi Caboni, Angelo Frongia, Nicola Melis, Lorenza Ghisu

المصدر: Tetrahedron. 72:8201-8209

مصطلحات موضوعية: Cyclobutanes, 010405 organic chemistry, Chemistry, Stereochemistry, Yield (chemistry), Organic Chemistry, Drug Discovery, Sigmatropic reaction, 010402 general chemistry, 01 natural sciences, Biochemistry, 0104 chemical sciences, Tryptamines

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::600bbc19be0ee5f2904200e3553170e0
https://doi.org/10.1016/j.tet.2016.10.024

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3

Stereoselective aza-Michael addition of anilines to 1-nitro cyclohexene by intramolecular protonation

المؤلفون: Angelo Frongia, Francesco Secci, Lorenza Ghisu, Nicola Melis

المصدر: Tetrahedron Letters. 56:6409-6412

مصطلحات موضوعية: Nitrile, Stereochemistry, Organic Chemistry, Enantioselective synthesis, Cyclohexene, Protonation, Biochemistry, Medicinal chemistry, chemistry.chemical_compound, chemistry, Intramolecular force, Organocatalysis, Drug Discovery, Michael reaction, Nitronate

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::4ca4b69f8e12c2e2496c6c14a3642d54
https://doi.org/10.1016/j.tetlet.2015.09.138

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4

Catalytic Enantioselective Synthesis of α-(Benzylamino)cyclobutanones

المؤلفون: David J. Aitken, Nicola Melis, Pierluigi Caboni, Régis Guillot, Angelo Frongia, Lorenza Ghisu, Francesco Secci

المصدر: European Journal of Organic Chemistry. 2015:4358-4366

مصطلحات موضوعية: Reaction sequence, Tandem, Chemistry, Stereochemistry, Intramolecular force, Organic Chemistry, Enantioselective synthesis, Physical and Theoretical Chemistry, Combinatorial chemistry, Tautomer, Catalysis

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::da055e17a5e2ab77dd03e9544a659a3f
https://doi.org/10.1002/ejoc.201500460

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5

Synthesis of 2,2-bis(pyridin-2-yl amino)cyclobutanols and their conversion into 5-(pyridin-2-ylamino)dihydrofuran-2(3H)-ones

المؤلفون: Nicola Melis, Thomas Boddaert, Régis Guillot, Lorenza Ghisu, David J. Aitken, Pierluigi Caboni, Massimiliano Arca, Angelo Frongia, Francesco Secci

المصدر: Organicbiomolecular chemistry. 15(46)

مصطلحات موضوعية: chemistry.chemical_compound, chemistry, 010405 organic chemistry, Organic Chemistry, Periodinane, Organic chemistry, Physical and Theoretical Chemistry, 010402 general chemistry, Ring (chemistry), 01 natural sciences, Biochemistry, Medicinal chemistry, 0104 chemical sciences

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48b0bc4a6d12570348f0cecbcfc323a8
https://pubmed.ncbi.nlm.nih.gov/29135013

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6

Enantioselective Heterogeneous Synergistic Catalysis for Asymmetric Cascade Transformations

المؤلفون: Niklas Hedin, Zoltán Bacsik, Lorenza Ghisu, Samson Afewerki, Armando Córdova, Eric V. Johnston, Oscar Verho, Luca Deiana

المصدر: Advanced Synthesis & Catalysis. 356:2485-2492

مصطلحات موضوعية: Metal, Nucleophile, Cascade, Chemistry, visual_art, Electrophile, visual_art.visual_art_medium, Enantioselective synthesis, Organic chemistry, Synergistic catalysis, General Chemistry, Catalysis

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::504606a569dd1eb3b11c671c17661134
https://doi.org/10.1002/adsc.201400291

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7

Efficient and Highly Enantioselective Aerobic Oxidation–Michael–Carbocyclization Cascade Transformations by Integrated Pd(0)-CPG Nanoparticle/Chiral Amine Relay Catalysis

المؤلفون: Lorenza Ghisu, Renyun Zhang, Oscar Córdova, Armando Córdova, Luca Deiana, Samson Afewerki

المصدر: Synthesis. 46:1303-1310

مصطلحات موضوعية: Allylic rearrangement, Cascade, Chemistry, Organic Chemistry, Enantioselective synthesis, Nanoparticle, Organic chemistry, Homogeneous catalysis, Chiral amine, Catalysis, Stereocenter

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::73415a1db8b11a0be846a1a4e5374d7b
https://doi.org/10.1055/s-0033-1340883

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8

Academic Journal

Synthesis of 2,2-bis(pyridin-2-yl amino)cyclobutanols and their conversion into 5-(pyridin-2-ylamino)dihydrofuran-2(3: H)-ones

المؤلفون: Lorenza Ghisu, Nicola Melis, Francesco Secci, Pierluigi Caboni, Massimiliano Arca, Regis Guillot, Thomas Boddaert, David J. Aitken, Angelo Frongia

المساهمون: Ghisu, Lorenza, Melis, Nicola, Secci, Francesco, Caboni, Pierluigi, Arca, Massimiliano, Guillot, Regi, Boddaert, Thoma, Aitken, David J., Frongia, Angelo

Relation: info:eu-repo/semantics/altIdentifier/pmid/29135013; info:eu-repo/semantics/altIdentifier/wos/WOS:000416538100004; volume:15; issue:46; firstpage:9779; lastpage:9784; numberofpages:6; journal:ORGANIC & BIOMOLECULAR CHEMISTRY; http://hdl.handle.net/11584/234137; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85036658068

الاتاحة: http://hdl.handle.net/11584/234137
https://doi.org/10.1039/c7ob02567j

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