Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Caterina Zoni"'
Autor:
Alessandro Contini, Gaetano Zecchi, Egle M. Beccalli, Ivan De Marchi, Caterina Zoni, Gianluigi Broggini
Publikováno v:
Tetrahedron: Asymmetry. 15:3181-3187
Enantiopure polyfunctionalized imidazo[1,2- a ]pyridines and pyrrolo[1,2- a ]imidazoles, two classes of heterocyclic compounds including anti-inflammatories and glycosidase inhibitors, were synthesized starting from natural α-aminoacids and exploiti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ff2bf6e2a0f92b2748417e03dd8579e
https://doi.org/10.1016/j.tetasy.2004.07.065
https://doi.org/10.1016/j.tetasy.2004.07.065
Publikováno v:
Organic Preparations and Procedures International. 35:609-613
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8af0294a8a0a62a0b4d4e9e8159eb380
https://doi.org/10.1080/00304940309355361
https://doi.org/10.1080/00304940309355361
Publikováno v:
ChemInform. 36
Starting from commercially available pyrrole- and thiophene-2-carboxylic acids 1 or thiophene- and furan-3-carboxylic acids 6, we report the synthesis of tricyclic fused quinolone and naphthyridone derivatives, in only three steps, by an intramolecul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fea05bbbd94bde43fa229f02bb52cc62
https://doi.org/10.1002/chin.200539138
https://doi.org/10.1002/chin.200539138
An original synthetic route toward dibenzo[b,e][1,4]diazepin-11-ones and analogues pyridobenzodiazepinones has been developed. The method relies upon an intramolecular amination process between an (hetero)aryl halide and the appropriate aniline moiet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37bc3b30c03ac65ecdf75f10150fce80
http://hdl.handle.net/11383/1495102
http://hdl.handle.net/11383/1495102
Publikováno v:
ChemInform. 35
A new synthesis of quinoline derivatives was achieved by catalytic hydrogenation of 3,4-disubstituted 2-(2-formylphenyl)-isoxazolin-5(2H)-ones. In the same way, 2,3-disubstituted [1,8]naphthyridine was obtained.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8890d91006bd1d804aa845ad1c54a3a2
https://doi.org/10.1002/chin.200413107
https://doi.org/10.1002/chin.200413107
Indole 2-carboxamide derivatives 4 underwent palladium-catalyzed intramolecular cyclization reactions to afford beta-carbolinones or pyrazino[1,2-a]indoles according to different reaction pathways. The complete regioselectivity of the reactions was o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::191d504d21b4379a8bb2a8fa27c9245e
http://hdl.handle.net/11383/1485950
http://hdl.handle.net/11383/1485950
Publikováno v:
European Journal of Organic Chemistry; May2005, Vol. 2005 Issue 10, p2091-2096, 6p
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd14c1c1bb22cc75c444da403b0b6b75
http://www.scopus.com/inward/record.url?eid=2-s2.0-0942289800&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0942289800&partnerID=MN8TOARS