222555-96-6Relevant articles and documents
Sugar-based novel chiral macrocycles for inclusion applications and chiral recognition
Singh, Ankita,Khatri, Vinod,Malhotra, Shashwat,Prasad, Ashok K.
, p. 25 - 32 (2016)
A convergent template assisted synthesis of sugar-based chiral macrocycles has been achieved. The host-guest inclusion studies have revealed significant interactions of the synthesized macrocycle with primary over secondary ammonium salt. The chiral macrocyle also discriminates between D- and L-phenylalanine methyl ester hydrochlorides as revealed by 1H NMR spectral studies on the mixture of the host and the guest molecules.
Hydrolytically stable arabinofuranoside analogs for the synthesis of arabinosyltransferase inhibitors
Chaumontet, Manon,Pons, Valérie,Marotte, Karine,Prandi, Jacques
, p. 1113 - 1116 (2007/10/03)
The first members of two new families of arabinosyltransferase inhibitors, derived from previously reported hybrid compounds covalently associating an iminoalditol with an α-d-arabinofuranoside, have been prepared. In place of the arabinofuranoside moiety
First synthesis of methyl α-C-D-arabinofuranosyl-(1→5)-α-D-arabinofuranoside: The C-disaccharide segment of motif C of Mycobacterium tuberculosis
Gurjar, Mukund K.,Nagaprasad, Ravi,Ramana
, p. 7577 - 7579 (2007/10/03)
The synthesis of C-analogue of the disaccharide 2 α-araf-(1→5)-araf, present in motif C of the arabino-galactan portion of Mycobacterium tuberculosis, has been described. The critical C-C bond formation reaction to couple both the furanosyl residues has b