Cyanuric chloride catalyzed Beckmann rearrangement of ketoximes in biodegradable ionic liquids

Autor: Dario Landini, Angelamaria Maia, Domenico Albanese

Publikováno v: Tetrahedron. 68:1947-1950

Imidazolium-based ionic liquids (ILs) containing ester moieties in the side chain were successfully used as an alternative to traditional ILs in the Beckmann rearrangement of ketoximes catalyzed by 2,4,6-trichloro[1,3,5]triazine. The procedure is mil

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4f1800c07dc4e86da8a7dbec694ca476
https://doi.org/10.1016/j.tet.2011.12.051

Complementary Heterogeneous/Homogeneous Protocols for the Synthesis of Densely Functionalized Benzo[d]sultams: C−C Bond Formation by Intramolecular Nucleophilic Aromatic Fluorine Displacement

Autor: Dario Landini, Domenico Albanese, Michele Penso, Vittoria Lupi, Aaron Tagliabue

Publikováno v: The Journal of Organic Chemistry. 73:6686-6690

Polyfunctionalized benzo[d]sultams 7 and 8, which contain an alpha-amino acid unit, have been synthesized from the corresponding open chain (pentafluorobenzene)sulfonamides 4 by complementary solid-liquid phase transfer catalysis (SL-PTC) and homogen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c8b0d0457f64a3a6b074c28f9ef5cba
https://doi.org/10.1021/jo800930g

Characterizing Ionic Liquids as Reaction Media through a Chemical Probe

Autor: Dario Landini, Cecilia Betti, Angelamaria Maia, Valentina Dichiarante, Angelo Albini, Maurizio Fagnoni

Publikováno v: 13 (2007): 1834–1841.
info:cnr-pdr/source/autori:Dichiarante, V.; Betti, C.; Fagnoni, M.; Maia, A.; Landini, D.; Albini, A./titolo:Characterizing Ionic Liquids as Reaction Media through a Chemical Probe/doi:/rivista:/anno:2007/pagina_da:1834/pagina_a:1841/intervallo_pagine:1834–1841/volume:13

The triplet N,N-dimethylaminophenyl cation, a highly reactive but chemospecific electrophile, has been used as a probe for characterizing the properties of reaction media for a series of imidazolium ILs. With the N-hexyl-N-methyl imidazolium derivati

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01dd8fb0d362e6c296ee8d8b9a966b70
https://doi.org/10.1002/chem.200601078

Chemoselective N-Alkylation of Di-N,O-protected Tyrosine through Specific Oxy-Anion Solvation by Non-Hydrogen Bonding Donor Solvents

Autor: Domenico Albanese, Michele Penso, Dario Landini, Davide Scaletti, Vittoria Lupi

Publikováno v: Synlett. :0741-0744

N-(2-Nitro-benzenesulfonyl) activated L-tyrosine methyl ester has been directly N-alkylated under solid-liquid phase-transfer catalysis (SL-PTC) conditions and in a coordinating non-hydrogen bonding donor (non-HBD) solvent, which reduces through spec

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8bc5c1110e02c3aa49f5881c5c106be0
https://doi.org/10.1055/s-2006-932494

Synthesis of 2,6-disubstituted morpholines through regioselective oxiranes ring opening by tosylamide under PTC conditions

Autor: Davide Scaletti, Domenico Albanese, Michele Penso, Vittoria Lupi, Dario Landini

Publikováno v: Tetrahedron. 60:11709-11718

Symmetric and non-symmetric 2,6-disubstituted morpholines were synthesized through regioselective nucleophilic ring opening of oxiranes with tosylamide under solid–liquid phase transfer catalysis (SL-PTC) conditions followed by cyclization of the t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eadbf3fc49cef58c75063f5be4a01bda
https://doi.org/10.1016/j.tet.2004.10.008