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Akademický článek
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Akademický článek
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Autor:
Vaghi, L., Benincori, T., Cirilli, R., Alberico, E., Mussini, P. R., Pierini, Marco, Pilati, T., Rizzo, S., Sannicolò, F.
Publikováno v:
European journal of organic chemistry (Online) (2013). doi:10.1002/ejoc.201301098
info:cnr-pdr/source/autori:Vaghi Luca, Benincori Tiziana, Cirilli Roberto, Elisabetta Alberico, Mussini Romana Patrizia, Pierini Marco, Pilati Tullio, Rizzo Simona, Francesco Sannicolo/titolo:Ph-tetraMe-Bithienine, the First Member of the Class of Chiral Heterophosphepines: Synthesis, Electronic and Steric Properties, Metal Complexes and Catalytic Activity/doi:10.1002%2Fejoc.201301098/rivista:European journal of organic chemistry (Online)/anno:2013/pagina_da:/pagina_a:/intervallo_pagine:/volume
info:cnr-pdr/source/autori:Vaghi Luca, Benincori Tiziana, Cirilli Roberto, Elisabetta Alberico, Mussini Romana Patrizia, Pierini Marco, Pilati Tullio, Rizzo Simona, Francesco Sannicolo/titolo:Ph-tetraMe-Bithienine, the First Member of the Class of Chiral Heterophosphepines: Synthesis, Electronic and Steric Properties, Metal Complexes and Catalytic Activity/doi:10.1002%2Fejoc.201301098/rivista:European journal of organic chemistry (Online)/anno:2013/pagina_da:/pagina_a:/intervallo_pagine:/volume
Unknown 1H-2,7-dihydro-1-phenylphosphepine, containing a 2,2,5,5-tetramethyl-3,3-bithiophene atropisomeric scaffold (Ph-tetraMe- Bithienine), and its oxide have been synthesized and structurally characterized by single-crystal X-ray diffraction analy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4ffaea66e4c2300289e2823fe2500421
http://hdl.handle.net/11383/1921523
http://hdl.handle.net/11383/1921523
Publikováno v:
Journal of molecular catalysis. A, Chemical (Online) 363-364 (2012): 49–57.
info:cnr-pdr/source/autori:Grabulosa A., Mannu A., Alberico E., Denurra S., Gladiali S., Muller. G./titolo:Neutral p6-arene ruthenium complexes with monodentate P-donor ligands: Activation in the transfer hydrogenation reaction/doi:/rivista:Journal of molecular catalysis. A, Chemical (Online)/anno:2012/pagina_da:49/pagina_a:57/intervallo_pagine:49–57/volume:363-364
info:cnr-pdr/source/autori:Grabulosa A., Mannu A., Alberico E., Denurra S., Gladiali S., Muller. G./titolo:Neutral p6-arene ruthenium complexes with monodentate P-donor ligands: Activation in the transfer hydrogenation reaction/doi:/rivista:Journal of molecular catalysis. A, Chemical (Online)/anno:2012/pagina_da:49/pagina_a:57/intervallo_pagine:49–57/volume:363-364
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b6c25c0e2f36a0351af4f4823da4be77
http://www.cnr.it/prodotto/i/191837
http://www.cnr.it/prodotto/i/191837
Autor:
S. Rizzo, S., Benincori, T., Bonometti, V., Cirilli, R., Ferretti, R., Mussini, P., Pierini, M., Pilati, T., Sannicolò, F., Vaghi L., Alberico, E.
Publikováno v:
X Congresso del Gruppo Interdivisionale di Chimica Organometallica della SCI, Padova (Italy), 5-8 Giugno 2012
info:cnr-pdr/source/autori:S. Rizzo, S.; Benincori, T.; Bonometti, V.; Cirilli, R.; Ferretti, R.; Mussini, P.; Pierini, M.; Pilati, T.; Sannicolò, F.; Vaghi L.; Alberico, E./congresso_nome:X Congresso del Gruppo Interdivisionale di Chimica Organometallica della SCI/congresso_luogo:Padova (Italy)/congresso_data:5-8 Giugno 2012/anno:2012/pagina_da:/pagina_a:/intervallo_pagine
info:cnr-pdr/source/autori:S. Rizzo, S.; Benincori, T.; Bonometti, V.; Cirilli, R.; Ferretti, R.; Mussini, P.; Pierini, M.; Pilati, T.; Sannicolò, F.; Vaghi L.; Alberico, E./congresso_nome:X Congresso del Gruppo Interdivisionale di Chimica Organometallica della SCI/congresso_luogo:Padova (Italy)/congresso_data:5-8 Giugno 2012/anno:2012/pagina_da:/pagina_a:/intervallo_pagine
Over the last few years the metal complexes of a wide range of monodentate P-donor ligands has been proved to equal or even to outperform their analogous bidentate counterparts in some asymmetric reactions.1 A crucial role is played by the electronic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::d70c2183081d6a8b7ed6fb774b3ced8f
https://publications.cnr.it/doc/195213
https://publications.cnr.it/doc/195213
Publikováno v:
Chemical communications (Lond., 1996, Online) 48 (2012): 2186–2188.
info:cnr-pdr/source/autori:Gridnev, I. D., Alberico E., Gladiali S./titolo:Captured at last: a Catalyst-Substrate Adduct and Rh-dihydride solvate in the Asymmetric Hydrogenation by a Rh-Monophosphine Catalyst/doi:/rivista:Chemical communications (Lond., 1996, Online)/anno:2012/pagina_da:2186/pagina_a:2188/intervallo_pagine:2186–2188/volume:48
info:cnr-pdr/source/autori:Gridnev, I. D., Alberico E., Gladiali S./titolo:Captured at last: a Catalyst-Substrate Adduct and Rh-dihydride solvate in the Asymmetric Hydrogenation by a Rh-Monophosphine Catalyst/doi:/rivista:Chemical communications (Lond., 1996, Online)/anno:2012/pagina_da:2186/pagina_a:2188/intervallo_pagine:2186–2188/volume:48
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::9b16a0f32fdcbef58590ac86caee83a9
http://www.cnr.it/prodotto/i/190137
http://www.cnr.it/prodotto/i/190137
Publikováno v:
Dalton transactions (2003. Online) 41 (2012): 8813–8821.
info:cnr-pdr/source/autori:Monney A., Alberico E., Ortin Y., Müller-Bunz H., Gladiali S., Albrecht M./titolo:Stereospecific synthesis and catalytic activity of L-histidylidene metal complexes/doi:/rivista:Dalton transactions (2003. Online)/anno:2012/pagina_da:8813/pagina_a:8821/intervallo_pagine:8813–8821/volume:41
info:cnr-pdr/source/autori:Monney A., Alberico E., Ortin Y., Müller-Bunz H., Gladiali S., Albrecht M./titolo:Stereospecific synthesis and catalytic activity of L-histidylidene metal complexes/doi:/rivista:Dalton transactions (2003. Online)/anno:2012/pagina_da:8813/pagina_a:8821/intervallo_pagine:8813–8821/volume:41
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::35b15063c98f60e53d303547baf3a1c8
http://www.cnr.it/prodotto/i/190139
http://www.cnr.it/prodotto/i/190139
Dimethoxydibenzophosphepine: a Novel Axially Chiral Monophosphane for Efficient Asymmetric Catalysis
Publikováno v:
ChemCatChem
2 (2010): 1395–1398.
info:cnr-pdr/source/autori:Alberico E., Karandikar S., Gladiali S./titolo:Dimethoxydibenzophosphepine: a Novel Axially Chiral Monophosphane for Efficient Asymmetric Catalysis/doi:/rivista:ChemCatChem (Print)/anno:2010/pagina_da:1395/pagina_a:1398/intervallo_pagine:1395–1398/volume:2
2 (2010): 1395–1398.
info:cnr-pdr/source/autori:Alberico E., Karandikar S., Gladiali S./titolo:Dimethoxydibenzophosphepine: a Novel Axially Chiral Monophosphane for Efficient Asymmetric Catalysis/doi:/rivista:ChemCatChem (Print)/anno:2010/pagina_da:1395/pagina_a:1398/intervallo_pagine:1395–1398/volume:2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::93ed9c5238e00779792d2a99dd9b72f9
http://www.cnr.it/prodotto/i/16110
http://www.cnr.it/prodotto/i/16110
Publikováno v:
COST Chemistry D40 Innovative Catalysis: New Processes and Selectivities, Ankara, 2010
info:cnr-pdr/source/autori:Besnea M., Parvulescu V. I., Hren J., Kocevar M., Richards R., Alberico E., S. Gladiali/congresso_nome:COST Chemistry D40 Innovative Catalysis: New Processes and Selectivities/congresso_luogo:Ankara/congresso_data:2010/anno:2010/pagina_da:/pagina_a:/intervallo_pagine
info:cnr-pdr/source/autori:Besnea M., Parvulescu V. I., Hren J., Kocevar M., Richards R., Alberico E., S. Gladiali/congresso_nome:COST Chemistry D40 Innovative Catalysis: New Processes and Selectivities/congresso_luogo:Ankara/congresso_data:2010/anno:2010/pagina_da:/pagina_a:/intervallo_pagine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::cea1f91fc022142740cb69365b715002
http://www.cnr.it/prodotto/i/104955
http://www.cnr.it/prodotto/i/104955
Publikováno v:
Tetrahedron: asymmetry
21 (2010): 1406–1410. doi:10.1016/j.tetasy.2010.04.031
info:cnr-pdr/source/autori:Alberico E.; Gladiali S.; Taras R.; Junge K.; Beller M.;/titolo:Expanding the scope of atropisomeric monodentate P-donor ligands in asymmetric catalysis. Asymmetric allylic alkylation of 1,3-diphenyl-2-propenyl-1-esters by Pd%2F BINEPINE catalysts/doi:10.1016%2Fj.tetasy.2010.04.031/rivista:Tetrahedron: asymmetry (Print)/anno:2010/pagina_da:1406/pagina_a:1410/intervallo_pagine:1406–1410/volume:21
21 (2010): 1406–1410. doi:10.1016/j.tetasy.2010.04.031
info:cnr-pdr/source/autori:Alberico E.; Gladiali S.; Taras R.; Junge K.; Beller M.;/titolo:Expanding the scope of atropisomeric monodentate P-donor ligands in asymmetric catalysis. Asymmetric allylic alkylation of 1,3-diphenyl-2-propenyl-1-esters by Pd%2F BINEPINE catalysts/doi:10.1016%2Fj.tetasy.2010.04.031/rivista:Tetrahedron: asymmetry (Print)/anno:2010/pagina_da:1406/pagina_a:1410/intervallo_pagine:1406–1410/volume:21
Monodentate binaphthophosphepines (BINEPINES) have been tested in the palladium-catalyzed asymmetric allylic alkylation of 1,3-diphenylallyl esters. Stereoselectivities of up to 92% ee have been achieved in the alkylation of the acetate ester with th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::cb1cf0637756366a749a6b5b9cd93929
http://www.cnr.it/prodotto/i/16108
http://www.cnr.it/prodotto/i/16108