Zobrazeno 1 - 10
of 310
pro vyhledávání: '"Orazio A. Attanasi"'
Autor:
Gianfranco Favi, Cristina Ciancimino, Barbara Parrino, Orazio A. Attanasi, Virginia Spanò, Anna Carbone
Publikováno v:
Molecules, Vol 18, Iss 3, Pp 2518-2527 (2013)
A series of substituted ethyl 1-[(tert-butoxycarbonyl)amino]-2-methyl-5- (1-methyl-1H-indol-3-yl)-4-[(1-methyl-1H-indol-3-yl)carbonyl]-1H-pyrrole-3-carboxylates were prepared in excellent yields (82-98%) by one-pot reactions between β-dicarbonyl com
Externí odkaz:
https://doaj.org/article/90999f6393c8488e8cf8098e2e000a10
Autor:
Orazio A. Attanasi, Lucia De Crescentini, Paolino Filippone, Fabio Mantellini, Stefania Santeusanio
Publikováno v:
ARKIVOC, Vol 2002, Iss 11, Pp 274-292 (2003)
Externí odkaz:
https://doaj.org/article/da22af42e88d4795b00c58691bbce2f4
Autor:
Alberto Cayuelas, Fabio Mantellini, Gianfranco Favi, Carmen Nájera, Serena Mantenuto, José M. Sansano, Orazio A. Attanasi
Publikováno v:
European Journal of Organic Chemistry. 2016:4144-4151
The Spanish authors thank the Spanish Ministerio de Ciencia e Innovacion (MICINN) (projects CTQ2010-20387, and Consolider Ingenio 2010, CSD2007-00006), the Spanish Ministerio de Economia y Competitividad (MINECO) (projects CTQ2013-43446-P, and CTQ201
Autor:
Gianfranco Favi, Fabio Mantellini, Francesca R. Perrulli, Lucia De Crescentini, Stefania Santeusanio, Orazio A. Attanasi
Publikováno v:
European Journal of Organic Chemistry. 2015:7154-7159
A mild, sequential multicomponent reaction strategy for the regioselective synthesis of functionalized pentasubstituted pyrroles from readily accessible primary amines, 1,2-diaza-1,3-dienes, and 2,3-allenoates, has been developed. The process allows
Autor:
Simona Nicolini, Fabio Mantellini, Giada Moscatelli, Gianfranco Favi, Orazio A. Attanasi, Serena Mantenuto
Publikováno v:
Synlett. 26:193-196
A regioselective inverse-electron-demand hetero-Diels–Alder reaction of in situ generated 1,2-diaza-1,3-dienes with methoxyallene is reported. These Lewis and Bronsted acid free reactions benefit from operational simplicity and allow access to sy
Autor:
Paolino Filippone, Gianluca Giorgi, Simona Nicolini, Francesca R. Perrulli, Stefania Santeusanio, Orazio A. Attanasi, Lucia De Crescentini
Publikováno v:
Tetrahedron. 70:7336-7343
A straightforward method for the synthesis of spaced, phenyl-linked bis(thiohydantoin) derivatives and (thio)hydantoins spiro-fused to pyrroline ring has been developed. All the synthetic strategies here presented rely on initial aza-Michael addition
Publikováno v:
Synlett. 25:2001-2004
Carbanions generated from various acyclic and cyclic α-azido ketones in the presence of bases were reacted with ethyl 3-[(carbamoylimino)amino]but-2-enoate as a Michael acceptor to give the corresponding adducts. The adducts of acyclic azides were u
Autor:
Gianfranco Favi, Luca Bianchi, Rocco Racioppi, Maurizio D'Auria, Orazio A. Attanasi, Fabio Mantellini
Publikováno v:
Current Organic Synthesis. 10:951-960
Autor:
Fabio Mantellini, Gianfranco Favi, Orazio A. Attanasi, Luca Bianchi, Lucia De Crescentini, Linda A. Campisi
Publikováno v:
Organic Letters. 15:3646-3649
A very simple domino reaction under solvent-free conditions of various pyridine-like heterocycles with 1,2-diaza-1,3-dienes produces in good yields imidazo[1,2-a]pyridines, imidazo[1,2-a]quinolines, and imidazo[2,1-a]isoquinolines. The advantage of t
Autor:
Fabio Mantellini, Giada Moscatelli, Gianfranco Favi, Orazio A. Attanasi, Aliki Paparisva, Athina Geronikaki
Publikováno v:
Organic Letters. 15:2624-2627
A domino reaction of vinyl malononitriles (VMs) with 1,2-diaza-1,3-dienes (DDs) produce unprecedented 3a,4-dihydro-1H-pyrrolo[1,2-b]pyrazole systems in a chemo-, regio-, and stereoselective fashion. This base promoted (DIPEA) one-pot transformation i