J.‐L. IMBACH

Combinatorially selected guanosine-quartet structureis a potent inhibitor of human immunodeficiency virus envelope-mediated cellfusion.

Jacqueline R. Wyatt, Timothy A. Vickers, Joseph L. Roberson et al. · Proceedings of the National Academy of Sciences · 1994 · 300 citations · Full text

Life Sciences, Medicinal Chemistry, Molecular Biology +17

Synthesis of 2',3'-differentiated ribonucleosides via glycosylation reactions with 2-O-Me or 2-O-TBDMS ribofuranose derivatives. 1. Pyrimidine series

Claude Chavis, Françoise Dumont, R. H. WIGHTMAN et al. · The Journal of Organic Chemistry · 1982 · 34 citations

Natural Sciences, Biochemistry, Chemistry +13

New insights regarding the potential of the pronucleotide approach in antiviral chemotherapy.

G. Gosselin, Jean‐Luc Girardet, Christian Périgaud et al. · Acta Biochimica Polonica · 1996 · 25 citations · Full text

Medicine, Molecular Biology, Pharmacology +16

Effect of the N-glycosidic bond conformation and modifications in the pentose moiety on the binding of nucleoside ligands to uridine phosphorylase.

Mahmoud H. el Kouni, Fardos N.M. Naguib, S. Haihua Chu et al. · Molecular Pharmacology · 1988 · 21 citations

Life Sciences, Biochemistry, Molecular Biology +15

Sugar modified oligonucleotides : II. Solid phase synthesis of nuclease resistant α-anomeric uridylates as potential antisense agents

Françoise Debart, Bernard Rayner, J.‐L. IMBACH · Tetrahedron Letters · 1990 · 18 citations · Full text

Pharmacy, Biotechnology, Molecular Biology +16