Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Monica Dell'Acqua"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 1997-2006 (2015)
A Lewis acid-catalysed diastereoselective [4 + 2] cycloaddition of vinylindoles and methyl 2-acetamidoacrylate, leading to methyl 3-acetamido-1,2,3,4-tetrahydrocarbazole-3-carboxylate derivatives, is described. Treatment of the obtained cycloadducts
Externí odkaz:
https://doaj.org/article/96180fb139e64b1b945945cd2c94b49b
Autor:
Donatella Nava, Stefano Peroni, Giorgio Abbiati, Valentina Pirovano, Elisabetta Rossi, Giorgio Tseberlidis, Monica Dell'Acqua
Publikováno v:
European Journal of Organic Chemistry. 2017:1425-1433
In this paper, we report the first example of silver triflate-catalyzed synthesis of 1,3-dicarbosubstituted isochromene derivatives starting from 2-alkynyl(hetero)arylaldehydes and enolizable ketones. The reaction proceeds in a cascade fashion under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97bfafbc9ee4507598bb0801e3813d37
https://doi.org/10.1002/ejoc.201601602
https://doi.org/10.1002/ejoc.201601602
Autor:
Giorgio Abbiati, Valentina Pirovano, Monica Dell'Acqua, Elisabetta Rossi, Elisa Arpini, Rubén Vicente
Publikováno v:
Advanced Synthesis & Catalysis. 358:403-409
A gold(I)-catalyzed cascade [3,3]-propargylic rearrangement and [4+2] cycloaddition reaction of 2-vinylindoles with propargylic esters is reported. The reaction leads to the synthesis of highly substituted tetrahydrocarbazole derivatives in high yiel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b002c561ce304ed83732f9bdfcaa0a7
https://doi.org/10.1002/adsc.201500913
https://doi.org/10.1002/adsc.201500913
Autor:
Alessandro Caselli, Emma Gallo, Giorgio Abbiati, Giorgio Tseberlidis, Elisabetta Rossi, Daniele Valcarenghi, Monica Dell'Acqua
Publikováno v:
RSC Advances. 6:97404-97419
We report herein the synthesis of new pyridine-containing macrocyclic ligands (Pc-L) bearing a non-innocent pendant arm, by exploiting both chiral and functional properties of natural amino acids. The obtained macrocyclic ligands were employed to syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f7c5dc28db2e94197d4d88bf5ba2c6b
https://doi.org/10.1039/c6ra22231e
https://doi.org/10.1039/c6ra22231e
Autor:
Monica Dell'Acqua, Giorgio Abbiati, Andrea Paganoni, Valentina Pirovano, Elisabetta Rossi, Marco Negrato
Publikováno v:
Organic & Biomolecular Chemistry. 14:6095-6110
A study on the SN2-type ring opening reactions of aziridines with indoles as nucleophiles is reported. Under gold(i) catalysis a great variety of tryptamine derivatives were prepared in good to excellent yields with complete stereocontrol when chiral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15d1f2fb51e2836240b57f1f507f202d
https://doi.org/10.1039/c6ob00672h
https://doi.org/10.1039/c6ob00672h
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 1997-2006 (2015)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry
A Lewis acid-catalysed diastereoselective [4 + 2] cycloaddition of vinylindoles and methyl 2-acetamidoacrylate, leading to methyl 3-acetamido-1,2,3,4-tetrahydrocarbazole-3-carboxylate derivatives, is described. Treatment of the obtained cycloadducts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d4892996f62181d045d0b2cab864ec2
https://doaj.org/article/96180fb139e64b1b945945cd2c94b49b
https://doaj.org/article/96180fb139e64b1b945945cd2c94b49b
Autor:
Clara Cecchini, Giorgio Abbiati, Valentina Pirovano, Alessandro Caselli, Elisabetta Rossi, B. Castano, Monica Dell'Acqua, Tommaso Pedrazzini
Publikováno v:
The Journal of Organic Chemistry. 79:3494-3505
The synthesis of 3-substituted-1-alkoxyisochromenes starting from 2-alkynylbenzaldehydes and different alcohols is reported. The reaction is catalyzed by a silver(I) complex with an original macrocyclic pyridine-containing ligand. The approach is cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5da45b2f7ff0f08c85ea21c3b7f5e09
https://doi.org/10.1021/jo5002559
https://doi.org/10.1021/jo5002559
Autor:
Monica Dell'Acqua, Diego Facoetti, Silvia Rizzato, Giorgio Abbiati, Donatella Nava, Valentina Pirovano, Elisabetta Rossi
Publikováno v:
European Journal of Organic Chemistry. 2013:6267-6279
The gold-catalyzed intermolecular Diels–Alder cycloaddition and competitive Michael addition reactions between 2-vinylindoles and enones/enals are reported. The reaction outcome strictly correlates with the electronic character of the heteroaromati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::feda2bf5272949c1e61325db8037ac20
https://doi.org/10.1002/ejoc.201300725
https://doi.org/10.1002/ejoc.201300725
Autor:
Giorgio Abbiati, Valentina Pirovano, Marco Negrato, Andrea Paganoni, Elisabetta Rossi, Monica Dell'Acqua
Publikováno v:
ChemInform. 47
A study on the SN2-type ring opening reactions of aziridines with indoles as nucleophiles is reported. Under gold(I) catalysis a great variety of tryptamine derivatives were prepared in good to excellent yields with complete stereocontrol when chiral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::878c1a3acffd65bfbd8ac087b1c21380
https://doi.org/10.1002/chin.201645113
https://doi.org/10.1002/chin.201645113
Publikováno v:
Organic letters. 18(19)
A new gold-catalyzed reaction of ynamides with 3-substituted indoles as nucleophiles is reported. The reaction allows for the synthesis of a new class of 2-vinylindole derivatives in good yields via the intermediacy of a cyclopropyl gold-carbenoid sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1d5278f56fd0361747ab76ae2784102
https://pubmed.ncbi.nlm.nih.gov/27612094
https://pubmed.ncbi.nlm.nih.gov/27612094