Authors: Peyrottes, S Schlienger, N Beltran, T Lefebvre, I Pompon, A Gosselin, G Aubertin, AM Imbach, JL Perigaud, C

Citation: S. Peyrottes et al., Design of new mononucleotide prodrugs: Aryl (SATE) phosphotriester derivatives, NUCLEOS NUC, 20(4-7), 2001, pp. 315-321

Authors: Beltran, T Egron, D Pompon, A Lefebvre, I Perigaud, C Gosselin, G Aubertin, AM Imbach, JL

Citation: T. Beltran et al., Rational design of a new series of pronucleotide, BIOORG MED, 11(13), 2001, pp. 1775-1777

Authors: Ribet, JP Zalavari, P Fahy, J Duflos, A Beltran, T

Citation: Jp. Ribet et al., Complete assignment of H-1 and C-13 NMR spectra of vinflunine, MAGN RES CH, 39(1), 2001, pp. 43-48

Authors: Beltran, T Egron, D Lefebvre, I Perigaud, C Pompon, A Gosselin, G Aubertin, AM Imbach, JL

Citation: T. Beltran et al., Anti-HIV pronucleotides: Sate versus phenyl as a protecting grow of AZT phosphoramidate derivatives, NUCLEOS NUC, 18(4-5), 1999, pp. 973-975

Authors: Alvarez, K Vasseur, JJ Beltran, T Imbach, JL

Citation: K. Alvarez et al., Photocleavable protecting groups as nucleobase protections allowed the solid-phase synthesis of base-sensitive SATE-prooligonucleotides, J ORG CHEM, 64(17), 1999, pp. 6319-6328