Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Riccardo Cari"'
Autor:
Antenucci, Achille, Bella, Marco, Riccardo, Cari, DI SABATO, Antonio, Moliterno, Mauro, Moretti, Erica, Puglisi, Antonio, Salvio, Riccardo, Celine, Sperandio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3686::575e51d805de017d7cfc096a13c26410
http://hdl.handle.net/11573/1340230
http://hdl.handle.net/11573/1340230
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
Autor:
Antenucci, Achille, Bella, Marco, Riccardo, Cari, DI SABATO, Antonio, Moliterno, Mauro, Moretti, Erica, Puglisi, Antonio, Salvio, Riccardo, Celine, Sperandio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3686::ce85aca7f2ec5570ae017178389fb983
http://hdl.handle.net/11573/1340216
http://hdl.handle.net/11573/1340216
Autor:
Polyssena Renzi, Alessandro Nicolosi, Diego Morra, Deborah Rosato, Marco Bella, Riccardo Cari, Cristiana Margarita, Daniele M. Scarpino Schietroma, Fabio Sciubba, Mattia Silvi, Alessio Vecchioni, Ivan Bordacchini
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 19(30)
A challenging asymmetric reaction (aza-Michael addition of imides to enones) has been optimized through an integrated approach involving the synthesis of a family of organocatalysts, multiple catalysis (usage of additives), and finally with rational
Autor:
Luciano Malchiodi, Alessandro Cucchi, Paolo Ghensi, Riccardo Caricasulo, Pier Francesco Nocini
Publikováno v:
Biotechnology & Biotechnological Equipment, Vol 30, Iss 4, Pp 762-769 (2016)
The aim of this multicentre prospective study was to evaluate the efficacy and safety of a surgical approach based on a novel osteotome technique, in order to obtain both alveolar ridge expansion and sinus floor elevation. Partially edentulous patien
Externí odkaz:
https://doaj.org/article/e59d27a6233149c2a4f82f62351a5b24