Zobrazeno 1 - 4
of 4
pro vyhledávání: '"M. Candida Cesta"'
Autor:
Roberto Curti, Valerio D'Elia, Marcello Allegretti, Gaetano D'Anniballe, Silvia Coniglio, Andrea Aramini, Giuseppe Nano, Valerie Orlando, Fabrizio D'Alessandro, M. Candida Cesta, Sandro Colagioia
Publikováno v:
Tetrahedron Letters. 45:5375-5378
A new, simple and efficient procedure for the preparation of secondary amides through internal condensation of acylmethanesulfonamides ammonium salts is described. The selective acylation of mixed primary–secondary amines could be an attractive app
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb9fed263ce513f0fac9fb6b2d6137c0
https://doi.org/10.1016/j.tetlet.2004.05.073
https://doi.org/10.1016/j.tetlet.2004.05.073
Autor:
Valerio Berdini, Alessandra Topai, Nicolini Luca, Marcello Allegretti, M. Candida Cesta, Roberto Curti
Publikováno v:
Tetrahedron Letters. 42:4257-4259
A palladium-catalysed reduction of ketones to primary amines by reaction with ammonium formate in aqueous methanol is described. The proposed method provides a one-pot synthesis of 3-endo-tropanamine in high yields and stereoselectivity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a6791b3b43ebf972228b332a3e5213b
https://doi.org/10.1016/s0040-4039(01)00663-3
https://doi.org/10.1016/s0040-4039(01)00663-3
Autor:
Valerio Berdini, M. Candida Cesta, Marcello Allegretti, Nicolini Luca, Roberto Curti, Alessandra Topai
Publikováno v:
ChemInform. 33
A palladium-catalysed reduction of ketones to primary amines by reaction with ammonium formate in aqueous methanol is described. The proposed method provides a one-pot synthesis of 3-endo-tropanamine in high yields and stereoselectivity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a6fa2d4500a71f81e57b29cb79cc398
https://doi.org/10.1002/chin.200213063
https://doi.org/10.1002/chin.200213063
Autor:
Roberto Curti, M. Candida Cesta, Giuseppe Zampella, Giuseppe Nano, Roberto Anacardio, Marco Mantovanini, Allegretti Marcello, and Alessandra Topai
An optimised cost-effective synthesis of the new antitussive drug, DF1012, is herewith reported. The new synthetic route to the key intermediate DF1005 is based on the unusual deprotection step of the 1-tert-butyl-3-cyano-7-azaindole intermediate, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e713306a1d6024e593edffb79579144
http://hdl.handle.net/10281/1240
http://hdl.handle.net/10281/1240
