Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Antonio Di Sabato"'
Publikováno v:
Chemical Science. 14:4923-4927
A photochemical organocatalytic method for the enantioselective incorporation of perfluoroalkyl and trifluoromethyl fragments at the remote γ position of α-branched enals is reported.
Autor:
Leonardo Straminelli, Francesco Vicentini, Antonio Di Sabato, Carmela Maria Montone, Chiara Cavaliere, Kari Rissanen, Francesca Leonelli, Fabrizio Vetica
Publikováno v:
The Journal of organic chemistry. 87(15)
A highly stereoselective procedure for the synthesis of spiro-polycyclic oxindoles bearing five contiguous stereogenic centers including two tetrasubstituted carbons has been developed. Under sequential organocatalysis performed by a pyrrolidine-base
Autor:
Antonio Di Sabato, Francesca D’Acunzo, Dario Filippini, Fabrizio Vetica, Antonio Brasiello, Davide Corinti, Enrico Bodo, Cinzia Michenzi, Edoardo Panzetta, Patrizia Gentili
Photocyclization of carbonyl compounds (known as the Norrish-Yang reaction) to yield cyclobutanols is, in general, accompanied by fragmentation reactions. The latter are predominant in the case of aldehydes so that secondary cyclobutanols are not con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ee6b0894e8f6c32cf1f50248516cd7b
https://hdl.handle.net/11573/1656147
https://hdl.handle.net/11573/1656147
Autor:
Francesca D'Acunzo, L. Mancini, Antonella Dalla Cort, Linda Carbonaro, Patrizia Gentili, Francesca Leonelli, Antonio Di Sabato, Dario Filippini
Publikováno v:
European journal of organic chemistry (Online) 2021 (2021): 289–294. doi:10.1002/ejoc.202001303
info:cnr-pdr/source/autori:D'Acunzo F.; Carbonaro L.; Cort A.D.; Di Sabato A.; Filippini D.; Leonelli F.; Mancini L.; Gentili P./titolo:Click-Connected 2-(Hydroxyimino)aldehydes for the Design of UV-Responsive Functional Molecules/doi:10.1002%2Fejoc.202001303/rivista:European journal of organic chemistry (Online)/anno:2021/pagina_da:289/pagina_a:294/intervallo_pagine:289–294/volume:2021
info:cnr-pdr/source/autori:D'Acunzo F.; Carbonaro L.; Cort A.D.; Di Sabato A.; Filippini D.; Leonelli F.; Mancini L.; Gentili P./titolo:Click-Connected 2-(Hydroxyimino)aldehydes for the Design of UV-Responsive Functional Molecules/doi:10.1002%2Fejoc.202001303/rivista:European journal of organic chemistry (Online)/anno:2021/pagina_da:289/pagina_a:294/intervallo_pagine:289–294/volume:2021
Click chemistry is used to functionalize simple lipophilic and water-soluble molecules, a complex PEGylated phospholipid (DSPE-PEG2000), and two benzylic substrates with the 2-(hydroxyimino)aldehyde (HIA) group. To this end, two terminal alkynes bear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4f54f9ded43fa41abb5bea0f03ee1e3
https://publications.cnr.it/doc/443302
https://publications.cnr.it/doc/443302
Autor:
Antonio Di Sabato, Achille Antenucci, Riccardo Salvio, Riccardo Cari, Antonio Puglisi, Marco Bella, Erica Moretti, Mauro Moliterno, Céline Sperandio
Publikováno v:
Angewandte Chemie (Int. ed., Print) 55 (2016): 6525–6529. doi:10.1002/anie.201601660
info:cnr-pdr/source/autori:Moliterno M.; Cari R.; Puglisi A.; Antenucci A.; Sperandio C.; Moretti E.; Di Sabato A.; Salvio R.; Bella M./titolo:Quinine-catalyzed asymmetric synthesis of 2,2?-binaphthol-type biaryls under mild reaction conditions/doi:10.1002%2Fanie.201601660/rivista:Angewandte Chemie (Int. ed., Print)/anno:2016/pagina_da:6525/pagina_a:6529/intervallo_pagine:6525–6529/volume:55
info:cnr-pdr/source/autori:Moliterno M.; Cari R.; Puglisi A.; Antenucci A.; Sperandio C.; Moretti E.; Di Sabato A.; Salvio R.; Bella M./titolo:Quinine-catalyzed asymmetric synthesis of 2,2?-binaphthol-type biaryls under mild reaction conditions/doi:10.1002%2Fanie.201601660/rivista:Angewandte Chemie (Int. ed., Print)/anno:2016/pagina_da:6525/pagina_a:6529/intervallo_pagine:6525–6529/volume:55
Simple quinine as an organocatalyst mediates the addition of various naphthols to halogenated quinones to afford non-C2 -symmetrical, axially chiral biaryl products, which are promising compounds as chiral ligands and organocatalysts. The rotational
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c260556e2595193147b493ac38056603
http://hdl.handle.net/2108/247695
http://hdl.handle.net/2108/247695