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- Synthesis and biological activity of analogues of vanchrobactin, a siderophore from Vibrio anguillarum serotype O2. Raquel G. Soengas, Marta Larrosa, Miguel Balado, Jaime Rodríguez, Manuel L. Lemos, Carlos Jiménez
, Org. Biomol. Chem.
, 2008
, 6
, 1278
- Epimerization of peptide nucleic acids analogs during solid-phase synthesis: optimization of the coupling conditions for increasing the optical purity. Roberto Corradini, Stefano Sforza, Arnaldo Dossena, Gerardo Palla, Raniero Rocchi, Ferdinando Filira, Flavia Nastri, Rosangela Marchelli
, J. Chem. Soc., Perkin Trans. 1
, 2001
, 2690
- Proton ionisation constants and kinetics of base hydrolysis of some α-amino-acid esters in aqueous solution. Part III. Hydrolysis and intramolecular aminolysis of αω-diamino-acid methyl esters. R. W. Hay, P. J. Morris
, J. Chem. Soc., Perkin Trans. 2
, 1972
, 1021
- Synthesis and mass spectra of some 3-acylamino-2-piperidones. D. R. Clarke, E. S. Waight
, J. Chem. Soc. C
, 1971
, 3743
- Chemoselective N-deacetylation under mild conditions. Prakash R. Sultane, Trimbak B. Mete, Ramakrishna G. Bhat
, Org. Biomol. Chem.
, 2014
, 12
, 261
- Reactions of copper(II) complexes of optically active N-substituted diamines with alk-3-en-2-ones or 4-hydroxyalkan-2-ones: formation of optically active macrocycles. Kazuo Miyamura, Kazuhiko Hata, Tadashi Makino, Masahiko Saburi, Sadao Yoshikawa
, J. Chem. Soc., Dalton Trans.
, 1987
, 1127
- 973. The formation of cyclic lactams from derivatives of basic amino-acids. B. C. Barrass, D. T. Elmore
, J. Chem. Soc.
, 1957
, 4830
- Total synthesis of Myxoprincomide, a secondary metabolite from Myxococcus xanthus. Michael Kohr, Christine Walt, Jan Dastbaz, Rolf Müller, Uli Kazmaier
, Org. Biomol. Chem.
, 2022
, 20
, 9609
- Inhibition and dispersion of Pseudomonas aeruginosa biofilms with reverse amide 2-aminoimidazole oroidin analogues. Justin J. Richards, T. Eric Ballard, Christian Melander
, Org. Biomol. Chem.
, 2008
, 6
, 1356
- Pyrrole carboxamide introduction in the total synthesis of pyrrole–imidazole alkaloids. Apsara K. Herath, Carl J. Lovely
, Org. Biomol. Chem.
, 2021
, 19
, 2603