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Results: 1-10 |
Results: 10
Scavenging of fluorinated N,N '-dialkylureas by hydrogen binding: A novel separation method for fluorous synthesis
Authors: Palomo, C Aizpurua, JM Loinaz, I Fernandez-Berridi, MJ Irusta, L
Citation: C. Palomo et al., Scavenging of fluorinated N,N '-dialkylureas by hydrogen binding: A novel separation method for fluorous synthesis, ORG LETT, 3(15), 2001, pp. 2361-2364
beta-lactams as versatile intermediates in alpha- and beta-amino acid synthesis
Authors: Palomo, C Aizpurua, JM Ganboa, I Oiarbide, M
Citation: C. Palomo et al., beta-lactams as versatile intermediates in alpha- and beta-amino acid synthesis, SYNLETT, (12), 2001, pp. 1813-1826
Diastereoselective Michael reactions of (1R)-(+)-camphor methyl ketone enolates with nitro olefins
Authors: Palomo, C Aizpurua, JM Oiarbide, M Garcia, JM Gonzalez, A Odriozola, I Linden, A
Citation: C. Palomo et al., Diastereoselective Michael reactions of (1R)-(+)-camphor methyl ketone enolates with nitro olefins, TETRAHEDR L, 42(29), 2001, pp. 4829-4831
On the question of the diastereoselective alkylation of 4-unsubstituted 3-amino beta-lactams. A concise synthesis of alpha-branched alpha-amino beta-lactams and their coupling with alpha-amino acid esters
Authors: Palomo, C Aizpurua, JM Galarza, R Benito, A Khamrai, UK Eikeseth, U Linden, A
Citation: C. Palomo et al., On the question of the diastereoselective alkylation of 4-unsubstituted 3-amino beta-lactams. A concise synthesis of alpha-branched alpha-amino beta-lactams and their coupling with alpha-amino acid esters, TETRAHEDRON, 56(31), 2000, pp. 5563-5570
Versatility of beta-lactams in synthesis. Studies directed toward the synthesis of complex nucleoside antibiotics and some macrocyclic peptides
Authors: Palomo, C Aizpurua, JM Ganboa, I Oiarbide, M
Citation: C. Palomo et al., Versatility of beta-lactams in synthesis. Studies directed toward the synthesis of complex nucleoside antibiotics and some macrocyclic peptides, PUR A CHEM, 72(9), 2000, pp. 1763-1768
Asymmetric synthesis of beta-lactams by Staudinger ketene-imine cycloaddition reaction
Authors: Palomo, C Aizpurua, JM Ganboa, I Oiarbide, M
Citation: C. Palomo et al., Asymmetric synthesis of beta-lactams by Staudinger ketene-imine cycloaddition reaction, EUR J ORG C, (12), 1999, pp. 3223-3235
alpha-alkyl-alpha-amino-beta-lactam peptides: Design, synthesis, and conformational features
Authors: Palomo, C Aizpurua, JM Benito, A Galarza, R Khamrai, UK Vazquez, J de Pascual-Teresa, B Nieto, PM Linden, A
Citation: C. Palomo et al., alpha-alkyl-alpha-amino-beta-lactam peptides: Design, synthesis, and conformational features, ANGEW CHEM, 38(20), 1999, pp. 3056-3058
From beta-lactams to alpha- and beta-amino acid derived peptides
Authors: Palomo, C Aizpurua, JM Ganboa, I Oiarbide, M
Citation: C. Palomo et al., From beta-lactams to alpha- and beta-amino acid derived peptides, AMINO ACIDS, 16(3-4), 1999, pp. 321-343
Diastereoselective conjugate reduction and enolate trapping with glyoxylate imines. A concise approach to beta-lactams that involves a ternary combination of components
Authors: Palomo, C Aizpurua, JM Gracenea, JJ
Citation: C. Palomo et al., Diastereoselective conjugate reduction and enolate trapping with glyoxylate imines. A concise approach to beta-lactams that involves a ternary combination of components, J ORG CHEM, 64(5), 1999, pp. 1693-1698
Highly diastereoselective aldol reactions with camphor-based acetate enolate equivalents
Authors: Palomo, C Oiarbide, M Aizpurua, JM Gonzalez, A Garcia, JM Landa, G Odriozola, I Linden, A
Citation: C. Palomo et al., Highly diastereoselective aldol reactions with camphor-based acetate enolate equivalents, J ORG CHEM, 64(22), 1999, pp. 8193-8200
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