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Mostrati risultati da 12 a 31 di 60
Titolo Data di pubblicazione Autore(i) File
Eco-friendly stereoselective reduction of alpha, beta-unsaturated carbonyl compounds by Er(OTf)O-3/NaBH4 in 2-MeTHF 1-gen-2015 Nardi, M; Sindona, Giovanni; Costanzo, P; Oliverio, M; Procopio, A.
Efficient synthesis of 9H-pyrrolo[1,2-a]indol-9-one derivatives based on active manganese dioxide promoted intramolecular cyclization 1-gen-2010 Aiello, Francesca; Garofalo, Antonio; Grande, Fedora
Efficient synthesis of isoxazolidine-substituted bisphosphonates by 1,3-dipolar cycloaddition reactions 1-gen-2011 Bortolini, O; Mulani, I; DE NINO, Antonio; Maiuolo, Loredana; Nardi, M; Russo, B; Avnet, S.
Exploration of synthetic strategies for the stereoselective preparation of novel tetrahydrofuran-containing biaryls: A high-pressure promoted Diels-Alder approach 1-gen-2018 Piazzolla, F.; Siciliano, C.; Minuti, L.; Temperini, A.
A facile one-pot synthesis of the very useful building blocks N-Boc-S-alkylatedcysteines 1-gen-1999 Cundari, S; Dalpozzo, Renato; DE NINO, Antonio; Procopio, A; Sindona, Giovanni; Athanassopulos, K.
Highly specific N-monomethylation of primary aromatic amines 1-gen-2006 LE PERA, A; Leggio, Antonella; Liguori, Angelo
MODEL STUDIES TOWARDS THE APPLICABILITY OF THE READILY AVAILABLE (S)-N-TRITYLASPARTIC ANHYDRIDE IN THE SYNTHESIS OF AMINO-ACIDS AND PEPTIDES 1-gen-1995 Athanassopoulos, C; Tzavara, C; Papaioannou, D; Sindona, Giovanni; Maia, Hls
Monomers containig substrate or inhibitor residues for copper amine oxidases and their hydrophilic beaded resins designed for enzyme interaction studied 1-gen-2004 Bertini, V; Alfei, S; Pocci, M; Lucchesini, F; Picci, N; Iemma, Francesca
Monomers containing substrate or inhibitor residues oxidases and their hydrophilic beaded resins designed for enzyme interaction studies 1-gen-2004 V., Bertini; S., Alfei; M., Pocci; F., Lucchesini; Picci, Nevio; F., Iemma
N,0-heterocyclics-12. Facile ring opening of some isoxazolidinium ions 1-gen-1983 Liguori, A; Sindona, Giovanni; Uccella, N.
N,O-Heterocyclics. 12. Facile Ring Opening of Some Isoxazolidinium Ions 1-gen-1983 Uccella, N; Liguori, Angelo; Sindona, G.
N,O-Heterocyclics. 14. Conversion of Isoxazolidines into a,ß-Enones 1-gen-1984 Uccella, N; Liguori, Angelo; Sindona, G.
N,O-heterocyclics13;-14conversion of isoxazolidines into α,β enones 1-gen-1984 Liguori, A; Sindona, Giovanni; Uccella, N.
N-alkylation of N-aryl-alpha-amino acid methyl esters by trialkyloxonium tetrafluoroborates 1-gen-2011 DE MARCO, R; DI GIOIA, M. L.; Liguori, Angelo; Perri, F; Siciliano, Carlo; Spinella, M.
N-Alkylation of N-arylsulfonyl-α-amino acid methyl esters by trialkyloxonium tetrafluoroborates 1-gen-2011 De Marco, R; DI GIOIA, Maria Luisa; Liguori, A; Perri, F; Siciliano, C; Spinella, M.
N-NOSYL-α-AMINO ACIDS IN THE SOLUTION PHASE PEPTIDE SYNTHESIS 1-gen-2007 DI GIOIA, M. L.; Leggio, A.; Liguori, Angelo; Perri, F.
N-Nosyl-α-Amino acids in the solution phase peptide synthesis 1-gen-2007 Leggio, Antonella; DI GIOIA, Maria Luisa; Perri, Francesca; Liguori, Angelo
New 2,3-dihydro-5h-1,4-benzodioxepin derivatives. Easy formation and x-ray structure determination of a pentacyclic acetal containing a fourteen-membered carbon-oxygen ring 1-gen-1995 Lucchesini, Francesco; Bertini, Vincenzo; Pocci, Marco; Munno, Giovanni De; Crispini, Alessandra
A new protocol for the synthesis of alpha',beta'-unsaturated 1,3-diketones 1-gen-1997 Dalpozzo, Renato; DE NINO, Antonio; Iantorno, E; Bartoli, G; Bosco, M; Sambri, L.
Novel approach to the ring-opening of 4-isoxazolines: one-pot synthesis of a,ß-enones 1-gen-1992 Uccella, N; Chiacchio, U; Liguori, Angelo; Rescifina, A; Romeo, G; Rossano, F; Sindona, G.
Mostrati risultati da 12 a 31 di 60
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