Sanajit Maiti and Balaram Mukhopadhyay
Org. Biomol. Chem., 2025,23, 1866-1873
Abstract
Conjugation of (S)-3-hydroxybutyric acid without terminal OH protection.
Andrea Lara-Pardo, Aurora Mancuso, Silvia Simón-Fuente, Paola M. Bonaccorsi, Chiara M. A. Gangemi, María Ángeles Moliné, Fausto Puntoriero, Maria Ribagorda, Anna Barattucci and Francisco Sanz-Rodriguez
Org. Biomol. Chem., 2023,21, 386-396
Abstract
Amino-OPE glycosides have been synthesized and tested as PSs in PDT under blue light.
Bedřich Formánek, Dorian Dupommier, Tereza Volfová, Silvie Rimpelová, Aneta Škarková, Jana Herciková, Daniel Rösel, Jan Brábek and Pavla Perlíková
RSC Med. Chem., 2024,15, 322-343
Abstract
Macrocyclic moiety is not essential for the biological activity of cytochalasan analogues.
Žaneta Javorská, Silvie Rimpelová, Magdaléna Labíková and Pavla Perlíková
Org. Biomol. Chem., 2024,22, 4536-4549
Abstract
Fe(acac)3-mediated late-stage arylation of cytochalasan analogues with Grignard reagents was developed.
Miqueas G. Traverssi, Verónica E. Manzano, Oscar Varela and Juan P. Colomer
RSC Adv., 2024,14, 2659-2672
Abstract
Synthesis of N-glycosyl amides is proposed from glycosyl azides. Hexose derivatives stereoselectively formed the β anomer, while xylo derivatives produced a mixture of α (1C4) and β (4C1) anomers. Free galactose derivatives were moderate inhibitors of E. coli β-galactosidase.