Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nadia Di Blasio"'
Autor:
Federico Berti, Carlo Bonini, Francesco Tramutola, Paolo Lupattelli, Rocco Pandolfo, Margherita De Bonis, Maria Funicello, Lucia Chiummiento, Nadia Di Blasio
Publikováno v:
Journal of Medicinal Chemistry. 53:1451-1457
A series of new thienyl ring containing analogues of nelfinavir and saquinavir with different substitution patterns were synthesized from suitable enantiopure diols. Their inhibitory activity against wild type recombinant HIV-1 protease was evaluated
Autor:
Jeremy N. Harvey, Varinder K. Aggarwal, Nadia Di Blasio, Olov A. Wallner, Xavier Ginesta, Guang Yu Fang
Publikováno v:
Journal of the American Chemical Society. 129:14632-14639
The reactions of aryl-stabilized sulfur ylides with organoboranes has been studied under a variety of conditions. At 5 or -78 degrees C, the reaction with Et3B gave a mixture of the first and second homologation products, but at -100 degrees C, only
Autor:
Arlette Solladié-Cavallo, Paolo Lupattelli, Milan Balaz, Nadia Di Blasio, Elias Choucair, Carlo Bonini
Publikováno v:
European Journal of Organic Chemistry. 2006:3007-3011
Amberlyst 15 is an efficient catalyst for the reaction of aryl-substituted oxiranes with acetone to prepare 2,2-dimethyl-1,3-dioxolanes in high yields. trans-2,3-Diaryloxiranes afford trans-acetonides enantiospecifically at room temperature, and the
Non-symmetrical trans-2,3-diaryloxiranes have been regioselectively opened by catalytic hydrogenation over Pd/C, NaBH4/Pd and [Cp2TiCl]/H2O. Although in the catalytic hydrogenation reactions the epoxides were mainly opened at the β-carbon with respe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a54c24853e8f2109cc118c70e47bc74
http://hdl.handle.net/11573/1653073
http://hdl.handle.net/11573/1653073
The trans-epoxide derivative of Combretastatin A-4 wasstereoselectively prepared in good yield by sulfur ylide mediated epoxidation of silyl-protected isovanillin. From this key intermediate, a formal synthesis of CA-4, by stereoselective deoxygenati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd66b9c3d7ebe3a90ff2a7ee8c4bf508
http://hdl.handle.net/11573/1653090
http://hdl.handle.net/11573/1653090