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1دورية أكاديمية
المؤلفون: Maria Rosaria Acocella, Rosaria Villano, Arrigo Scettri
المصدر: Molecules, Vol 14, Iss 8, Pp 3030-3036 (2009)
مصطلحات موضوعية: asymmetric Friedel-Crafts, indole, chiral phosphoric acids, Organic chemistry, QD241-441
وصف الملف: electronic resource
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المؤلفون: Arrigo Scettri, Maria Rosaria Acocella, Rosaria Villano
المصدر: ChemInform. 47
مصطلحات موضوعية: chemistry.chemical_classification, chemistry.chemical_compound, chemistry, Aldol reaction, Trimethylsilyl, Organocatalysis, Morpholine, Ether, General Medicine, Piperidine, Aldehyde, Medicinal chemistry, Kinetic resolution
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المؤلفون: Arrigo Scettri, Maria Rosaria Acocella, Rosaria Villano
المصدر: III Convegno dell'Istituto di Chimica Biomolecolare CNR, Catania, 28-30 Settembre 2016
info:cnr-pdr/source/autori:R. Villano, M. R. Acocella, A. Scettri/congresso_nome:III Convegno dell'Istituto di Chimica Biomolecolare CNR/congresso_luogo:Catania/congresso_data:28-30 Settembre 2016/anno:2016/pagina_da:/pagina_a:/intervallo_pagine
Tetrahedron (Oxf., Print) 72 (2016): 5414–5419. doi:10.1016/j.tet.2016.07.035
info:cnr-pdr/source/autori:Villano, Rosaria; Acocella, Maria Rosaria; Scettri, Arrigo/titolo:Influence of a remote sulfinyl group on L-proline-catalyzed direct asymmetric aldol addition of acetone/doi:10.1016%2Fj.tet.2016.07.035/rivista:Tetrahedron (Oxf., Print)/anno:2016/pagina_da:5414/pagina_a:5419/intervallo_pagine:5414–5419/volume:72مصطلحات موضوعية: Proline, Trimethylsilyl, Stereochemistry, asymmetric synthesis, Ether, 010402 general chemistry, 01 natural sciences, Biochemistry, Aldehyde, Kinetic resolution, chemistry.chemical_compound, Aldol reaction, Morpholine, Drug Discovery, polycyclic compounds, Chirality, Direct aldol reaction, Sulfinyl group, organocatalysis, L-proline, chemistry.chemical_classification, 010405 organic chemistry, organic chemicals, Organic Chemistry, 0104 chemical sciences, aldol addition, chemistry, Piperidine, Chirality (chemistry)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e66927a2b1bb253d920c2855cad4e794
http://www.cnr.it/prodotto/i/360825 -
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المصدر: Open Chemistry, Vol 10, Iss 1, Pp 47-53 (2012)
Central European Journal of Chemistry
info:cnr-pdr/source/autori:Arrigo Scettri; Rosaria Villano; Patrizia Manzo; Maria Rosaria Acocella/titolo:Mukaiyama-Michael vinylogous additions to nitroalkenes under solvent-free conditions/doi:10.2478%2Fs11532-011-0122-7/rivista:Central European Journal of Chemistry (Print)/anno:2012/pagina_da:47/pagina_a:53/intervallo_pagine:47–53/volume:10مصطلحات موضوعية: Solvent free, Chemistry, trimethylsilyloxyfuran, General Chemistry, Catalysis, Silyl ether, brønsted acids, chemistry.chemical_compound, Brønsted acids, Dioxinone-derived silyl ether, Nitroalkenes, Organocatalysis, Trimethylsilyloxyfuran, Yield (chemistry), dioxinone-derived silyl ether, Materials Chemistry, Organic chemistry, organocatalysis, nitroalkenes, Brønsted–Lowry acid–base theory, QD1-999, Conjugate
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::955fb583b29a22c2997df95de8b01a20
https://doi.org/10.2478/s11532-011-0122-7 -
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المؤلفون: Rosaria Villano, Arrigo Scettri, Maria Rosaria Acocella
المصدر: Tetrahedron (Oxf., Print) 67 (2011): 2768–2772.
info:cnr-pdr/source/autori:Rosaria Villano, Maria Rosaria Acocella, Arrigo Scettri/titolo:Synthesis of multifunctionalized building blocks via vinylogous addition of Chans diene to carbonyl and carbonyl-related electrophiles, mediated by molecular iodine/doi:/rivista:Tetrahedron (Oxf., Print)/anno:2011/pagina_da:2768/pagina_a:2772/intervallo_pagine:2768–2772/volume:67مصطلحات موضوعية: chemistry.chemical_classification, Chan's diene, Ketone, Diene, δ-Functionalized β-ketoesters, Organic Chemistry, Acetal, Imine, Biochemistry, Aldehyde, Chemical synthesis, Catalysis, Vinylogous reaction, chemistry.chemical_compound, γ-Selectivity, Iodine, chemistry, Drug Discovery, Electrophile, Organic chemistry
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المؤلفون: Laura Capozzolo, Antonio Massa, Arrigo Scettri
المصدر: Open Chemistry, Vol 8, Iss 6, Pp 1210-1215 (2010)
مصطلحات موضوعية: chemistry.chemical_classification, allylation of aldehydes, Dimethyl sulfoxide, organic chemicals, Aryl, sulfoxides, food and beverages, Substrate (chemistry), General Chemistry, lewis base, Aldehyde, Stannane, silicon tetrachloride, Catalysis, Chemistry, chemistry.chemical_compound, chemistry, Materials Chemistry, Silicon tetrachloride, Organic chemistry, allyltributylstannane, Lewis acids and bases, QD1-999
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74c444fa6ba22416de55ee4160afffe2
https://doi.org/10.2478/s11532-010-0099-7 -
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المصدر: 21 (2010): 1432.
info:cnr-pdr/source/autori:V. De Sio, M. R. Acocella, R. Villano, A. Scettri/titolo:New chiral imino-and amino-sulfoxides as activators of allyl trichlorosilane in the asymmetric allylation of aldehydes/doi:/rivista:/anno:2010/pagina_da:1432/pagina_a:/intervallo_pagine:1432/volume:21مصطلحات موضوعية: Inorganic Chemistry, Benzaldehyde, chemistry.chemical_compound, chemistry, Trichlorosilane, organic chemicals, Organic Chemistry, Organic chemistry, heterocyclic compounds, Physical and Theoretical Chemistry, Catalysis
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المؤلفون: Rosaria Villano, Maria Rosaria Acocella, Arrigo Scettri
المصدر: Molecules, Vol 14, Iss 8, Pp 3030-3036 (2009)
Molecules (Basel, Online) 14 (2009): 3030–3036. doi:10.3390/molecules14083030
info:cnr-pdr/source/autori:Arrigo Scettri, Rosaria Villano, Maria Rosaria Acocella/titolo:Asymmetric Friedel-Crafts Alkylation of Indole with Chalcones Catalyzed by Chiral Phosphoric Acids/doi:10.3390%2Fmolecules14083030/rivista:Molecules (Basel, Online)/anno:2009/pagina_da:3030/pagina_a:3036/intervallo_pagine:3030–3036/volume:14
Molecules; Volume 14; Issue 8; Pages: 3030-3036
Moleculesمصطلحات موضوعية: Indoles, Alkylation, Pharmaceutical Science, Article, Catalysis, Analytical Chemistry, Adduct, law.invention, lcsh:QD241-441, chemistry.chemical_compound, Chalcones, lcsh:Organic chemistry, law, Drug Discovery, Organic chemistry, chiral phosphoric acids, Phosphoric Acids, Physical and Theoretical Chemistry, Crystallization, Phosphoric acid, Friedel–Crafts reaction, Indole test, Molecular Structure, asymmetric Friedel-Crafts, indole, Organic Chemistry, Stereoisomerism, chemistry, Chemistry (miscellaneous), Yield (chemistry), Molecular Medicine
وصف الملف: application/pdf
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المؤلفون: Rosaria Villano, Rosanna Filosa, Vincenzo De Sio, M. Rosaria Acocella, Antonella Peduto, Giusi Sellitto, Laura Palombi, Paolo De Capraris, Antonio Massa, Arrigo Scettri
المساهمون: Massa, A, de Sio, V, Villano, R, Acocella, Mr, Palombi, L, Sellitto, G, Peduto, A, Filosa, Rosanna, De Capraris, P, Scettri, A.
المصدر: Synthesis (Stuttg.) (2009): 643–649. doi:10.1055/s-0028-1087677
info:cnr-pdr/source/autori:Antonio Massa, Vincenzo de Sio, Rosaria Villano, Maria Rosaria Acocella, Laura Palombi, Giusi Sellitto, Antonella Peduto, Rosanna Filosa, Paolo De Capraris, Arrigo Scettri/titolo:A new approach to di-and tetrasubstituted 2,3-dihydropyridin-4(1H)-ones through aza-Diels-Alder reaction promoted by silicon tetrachloride/doi:10.1055%2Fs-0028-1087677/rivista:Synthesis (Stuttg.)/anno:2009/pagina_da:643/pagina_a:649/intervallo_pagine:643–649/volumeمصطلحات موضوعية: heterocycles, Diene, Organic Chemistry, aza-Diels-Alder reaction, Alkylation, Catalysis, silicon tetrachloride, aza-Diels Alder reaction, chemistry.chemical_compound, chemistry, Silicon tetrachloride, Organic chemistry, Aza-Diels–Alder reaction, Derivative (chemistry), heterocycle
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::653da123c83c2b76c7d2546b3a0a2af4
https://doi.org/10.1055/s-0028-1087677 -
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المؤلفون: Alessandra Lattanzi, Arrigo Scettri, Sandro Piccirillo
المصدر: Advanced Synthesis & Catalysis. 349:357-363
مصطلحات موضوعية: Tandem, Enantioselective synthesis, chemistry.chemical_element, General Medicine, General Chemistry, Norcamphor, Combinatorial chemistry, Catalysis, Kinetic resolution, chemistry.chemical_compound, chemistry, Yield (chemistry), Organic chemistry, Chirality (chemistry), Titanium