Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Antonio D'Aurizio"'
Autor:
Mauro Panunzio, Elisa Bandini, Antonio D'Aurizio, Sha Long, Alessandro Venturini, Magda Monari
Publikováno v:
European journal of organic chemistry (Online) (2011): 6218–6225. doi:10.1002/ejoc.201100930
info:cnr-pdr/source/autori:Long, S. ; Monari, M. ; Panunzio, M.; Bandini, E. ; D'Aurizio, A.; Venturini, A./titolo:Hetero-Diels-Alder (HDA) Strategy for the Preparation of 6-Aryl-and Heteroaryl-Substituted Piperidin-2-one Scaffolds: Experimental and Theoretical Studies/doi:10.1002%2Fejoc.201100930/rivista:European journal of organic chemistry (Online)/anno:2011/pagina_da:6218/pagina_a:6225/intervallo_pagine:6218–6225/volume
info:cnr-pdr/source/autori:Long, S. ; Monari, M. ; Panunzio, M.; Bandini, E. ; D'Aurizio, A.; Venturini, A./titolo:Hetero-Diels-Alder (HDA) Strategy for the Preparation of 6-Aryl-and Heteroaryl-Substituted Piperidin-2-one Scaffolds: Experimental and Theoretical Studies/doi:10.1002%2Fejoc.201100930/rivista:European journal of organic chemistry (Online)/anno:2011/pagina_da:6218/pagina_a:6225/intervallo_pagine:6218–6225/volume
Preparation of piperidine-2-one scaffolds by the hetero-Diels-Alder (HAD) reaction, assisted by microwaves, is described. The versatility of this new approach has been demonstrated by the synthesis of racemic (+/-)-2-phenylpiperidine. Theoretical cal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91d7c6e384911a411f43ef9dbc6125fc
https://doi.org/10.1002/ejoc.201100930
https://doi.org/10.1002/ejoc.201100930
Publikováno v:
Synthetic Communications. 39:2151-2160
Microwave-assisted organic synthesis has been used for the cyclization of a monocyclic oxoamide to the corresponding bicyclic derivative via a Wittig-type coupling by means of phosphite reagents. The parameters influencing the reaction yields under m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::162acba63681f71e680bda0306f6782c
https://doi.org/10.1080/00397910802638586
https://doi.org/10.1080/00397910802638586
Publikováno v:
Synthesis. 2008:1753-1756
Hetero-Diels-Alder (HDA) methodology has been applied to the synthesis of Venlafaxine taking advantage of a novel MW-assisted transketalization and hydroxymethylation reaction.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e840bbe047a7c3bc45ac7f429ecaf76e
https://doi.org/10.1055/s-2008-1072581
https://doi.org/10.1055/s-2008-1072581
Autor:
Eileen Campana, Mauro Panunzio, Antonio D'Aurizio, Paola Vicennati, Emiliano Tamanini, Elisa Bandini
Publikováno v:
Tetrahedron (Oxf., Print) 62 (2006): 12270–12280. doi:10.1016/j.tet.2006.10.006
info:cnr-pdr/source/autori:Panunzio M.; Tamanini E.; Bandini E.; Campana E.; D'Aurizio A.; Vicennati P./titolo:5-Phenylthio-1,3-Oxazinan-4-Ones Via Hetero Diels-Alder Reactions: Synthesis Of (R)-And (S)-Duloxetines And Fluoxetines./doi:10.1016%2Fj.tet.2006.10.006/rivista:Tetrahedron (Oxf., Print)/anno:2006/pagina_da:12270/pagina_a:12280/intervallo_pagine:12270–12280/volume:62
info:cnr-pdr/source/autori:Panunzio M.; Tamanini E.; Bandini E.; Campana E.; D'Aurizio A.; Vicennati P./titolo:5-Phenylthio-1,3-Oxazinan-4-Ones Via Hetero Diels-Alder Reactions: Synthesis Of (R)-And (S)-Duloxetines And Fluoxetines./doi:10.1016%2Fj.tet.2006.10.006/rivista:Tetrahedron (Oxf., Print)/anno:2006/pagina_da:12270/pagina_a:12280/intervallo_pagine:12270–12280/volume:62
The synthesis of 5-phenylthio-1,3-oxazinan-4-ones, through a hetero Diels–Alder strategy, is described. The cycloadducts thus prepared have been shown to be useful intermediates for the synthesis of 1,3-aminoalcohols, valuable intermediates in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::203ffe44861e57afbb83cbb672a323ab
https://doi.org/10.1016/j.tet.2006.10.006
https://doi.org/10.1016/j.tet.2006.10.006
Publikováno v:
ChemInform. 40
Microwave-assisted organic synthesis has been used for the cyclization of a monocyclic oxoamide to the corresponding bicyclic derivative via a Wittig-type coupling by means of phosphite reagents. The parameters influencing the reaction yields under m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b371520ee5a93ba229088a6c425d1d78
https://doi.org/10.1002/chin.200944197
https://doi.org/10.1002/chin.200944197
Publikováno v:
Synthesis (Stuttg.)-(2007): 2060–2062. doi:10.1055/s-2007-965985
info:cnr-pdr/source/autori:Panunzio, M.; Bandini, E.; DAurizio, A.; Millemaggi, A.; Zhining Xia/titolo:EuFOD-Catalyzed Hetero-DielsAlder (HDA) Reaction under Microwave Heating/doi:10.1055%2Fs-2007-965985/rivista:Synthesis (Stuttg.)/anno:2007/pagina_da:2060/pagina_a:2062/intervallo_pagine:2060–2062/volume
info:cnr-pdr/source/autori:Panunzio, M.; Bandini, E.; DAurizio, A.; Millemaggi, A.; Zhining Xia/titolo:EuFOD-Catalyzed Hetero-DielsAlder (HDA) Reaction under Microwave Heating/doi:10.1055%2Fs-2007-965985/rivista:Synthesis (Stuttg.)/anno:2007/pagina_da:2060/pagina_a:2062/intervallo_pagine:2060–2062/volume
An efficient EuFOD-catalyzed hetero-Diels-Alder reaction between azadienes and aldehydes under microwave irradiation is reported. The reaction proceeds under microwave heating with 5 mol% of EuFOD in 45-83% yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::612153f8df9e9237776e01d5a941f8e5
https://doi.org/10.1002/chin.200747166
https://doi.org/10.1002/chin.200747166
Publikováno v:
Tetrahedron Letters. 51:933-934
Synthesis of optically active conhydrines has been achieved by hetero Diels–Alder cycloaddition assisted by microwaves.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ec79364402b4696e9a945280ea4295b
https://doi.org/10.1016/j.tetlet.2009.12.039
https://doi.org/10.1016/j.tetlet.2009.12.039