Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Andrea Fasana"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 8, Iss 1, Pp 1730-1746 (2012)
This review highlights the development of palladium-catalyzed C–H and N–H functionalization reactions involving indole derivatives. These procedures require unactivated starting materials and are respectful of the basic principle of sustainable c
Externí odkaz:
https://doaj.org/article/7ee0ddd4415e49bbb78e24b990afcac2
Autor:
Elena Borsini, Gianluigi Broggini, Andrea Fasana, Chiara Baldassarri, Angelo M. Manzo, Alcide D. Perboni
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 7, Iss 1, Pp 1468-1474 (2011)
In a simple procedure, the intramolecular hydroarylation of N-propargyl-pyrrole-2-carboxamides was accomplished with the aid of gold(III) catalysis. The reaction led to differently substituted pyrrolo[2,3-c]pyridine and pyrrolo[3,2-c]pyridine derivat
Externí odkaz:
https://doaj.org/article/bf34e47d261148f3a5d11fe36da88a74
Autor:
Vincenzina Barbera, Egle M. Beccalli, Ugo Chiacchio, Andrea Fasana, Silvia Gazzola, Simona Galli, Gianluigi Broggini
Publikováno v:
Advanced Synthesis & Catalysis. 355:1640-1648
Alkenylureas arising from glycine allylamides were proven to be suitable substrates for the synthesis of bicyclic five-membered ring-fused piperazinones. The reported intramolecular domino processes, performed under oxidative conditions with bis(acet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::469ab6046b2a2531f173e6cfc7cbd070
https://doi.org/10.1002/adsc.201300104
https://doi.org/10.1002/adsc.201300104
Publikováno v:
Journal of Organometallic Chemistry. 696:277-295
The formation of carbon–nitrogen bonds by reaction between a nitrogen atom and an unactivated carbon–hydrogen bond is a highly atom-economical process that attracted the attention of the chemists in the last two decades. The widely useful aminati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27ed326fbe75d9452269f8e1f193231d
https://doi.org/10.1016/j.jorganchem.2010.09.078
https://doi.org/10.1016/j.jorganchem.2010.09.078
Autor:
Ugo Chiacchio, Vincenzina Barbera, Silvia Gazzola, Egle M. Beccalli, Gianluigi Broggini, Simona Galli, Andrea Fasana
Publikováno v:
ChemInform. 44
Alkenylureas arising from glycine allylamides were proven to be suitable substrates for the synthesis of bicyclic five-membered ring-fused piperazinones. The reported intramolecular domino processes, performed under oxidative conditions with bis(acet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25f5f86e184ccf30c05553bf0af38a77
https://doi.org/10.1002/chin.201342170
https://doi.org/10.1002/chin.201342170
Publikováno v:
ChemInform. 44
This review highlights the development of palladium-catalyzed C–H and N–H functionalization reactions involving indole derivatives. These procedures require unactivated starting materials and are respectful of the basic principle of sustainable c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75125a366872b9810463c9c58aecf4af
https://doi.org/10.1002/chin.201308217
https://doi.org/10.1002/chin.201308217
Publikováno v:
ChemInform. 43
2-Vinyl- and 2-(α-styryl)quinazolin-4-ones have been synthesized by intramolecular gold-catalyzed hydroamination and palladium-catalyzed carboamination of anthranilic allenamides, easily prepared by prototropic isomerization of the corresponding pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e4fb35904dbd11a4d30d0fe72d76af5
https://doi.org/10.1002/chin.201248169
https://doi.org/10.1002/chin.201248169
2-Vinyl- and 2-(α-styryl)quinazolin-4-ones have been synthesized by intramolecular gold-catalyzed hydroamination and palladium-catalyzed carboamination of anthranilic allenamides, easily prepared by prototropic isomerization of the corresponding pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec18f54cd0411173efb1ac570beee8a1
http://hdl.handle.net/11383/1758236
http://hdl.handle.net/11383/1758236
Autor:
Simona Galli, Umberto Piarulli, Andrea Fasana, Maisaa Khansaa, Gianluigi Broggini, Elena Borsini, Micol Rigamonti
Publikováno v:
ChemInform. 42
Oxazolidinones fused to pyrazine or morpholine rings are prepared via aminocarboxylation reaction of allyl amides of N-alkoxycarbonyl-protected α-amino acids in the presence of stoichiometric CuCl2.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9560239b1da62ddfc07280700da95308
https://doi.org/10.1002/chin.201136167
https://doi.org/10.1002/chin.201136167
Publikováno v:
ChemInform. 42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a970ce1a67fd517c69b977dd5bfde74f
https://doi.org/10.1002/chin.201121161
https://doi.org/10.1002/chin.201121161