R. Vig

发表

Selectin ligands: 2,3,4-tri-O-acetyl-6-O-pivaloyl-α/β-galactopyranosyl halide as novel glycosyl donor for the synthesis of 3-O-sialyl or 3-O-sulfo Lex and Lea type structures

R. Jain, K. Matta, R. Locke, 1996 .

Selectin ligands: synthesis of 3′-O-sialyl-6′-O-sulfo Lewis, NeuAcα2→3(6-O-SO3Na)Galβ1→3 (Fucα1→4) GlcNAcβ–OMe

R. Jain, C. Piskorz, K. Matta, 1995 .

Non-nucleoside reverse transcriptase inhibitors for treatment of hiv infection

M. Uçkun, ChengYu Mao, R. Vig, 1999 .

Structure-based design of N-[2-(1-piperidinylethyl)]-N'-[2-(5-bromopyridyl)]-thiourea and N-[2-(1-piperazinylethyl)]-N'-[2-(5-bromopyridyl)]-thiourea as potent non-nucleoside inhibitors of HIV-1 reverse transcriptase.

F. Uckun, E. Sudbeck, T. Venkatachalam, 1998, Bioorganic & medicinal chemistry letters.

5-Alkyl-2-[(methylthiomethyl)thio]-6-(benzyl)-pyrimidin-4-(1H)-ones as potent non-nucleoside reverse transcriptase inhibitors of S-DABO series.

F. Uckun, E. Sudbeck, T. Venkatachalam, 1998, Bioorganic & medicinal chemistry letters.

Enhancing effects of a mono-bromo substitution at the para position of the phenyl moiety on the metabolism and anti-HIV activity of d4T-phenyl methoxyalaninyl phosphate derivatives.

F. Uckun, T. Venkatachalam, C. L. Chen, 1998, Bioorganic & medicinal chemistry letters.

Rational design and synthesis of phenethyl-5-bromopyridyl thiourea derivatives as potent non-nucleoside inhibitors of HIV reverse transcriptase

F. Uckun, E. Sudbeck, T. Venkatachalam, 1998 .

Selectin inhibition: synthesis and evaluation of novel sialylated, sulfated and fucosylated oligosaccharides, including the major capping group of GlyCAM-1.

A. Varki, R. Jain, A. Koenig, 1997, Glycobiology.

Synthesis of methyl O-(β-d-galactopyranosyl)-(1→3)-O-[α-l-fucopyranosyl-(1→4)]-2-acetamido-2-deoxy-6-O-sulfoβ -d-glucopyranoside sodium salt as a potential ligand for selectin molecules

R. Jain, K. Matta, R. Vig, 1995 .

Synthesis and antitumor activity of 1-β-D-arabinofuranosylcytosine conjugates of optical isomers of ether and thioether lipids

C. West, C. Hong, A. Nechaev, 1993, Lipids.

Structure-Based Design of Novel Dihydroalkoxybenzyloxopyrimidine Derivatives as Potent Nonnucleoside Inhibitors of the Human Immunodeficiency Virus Reverse Transcriptase

Rakesh Vig, Fatih M. Uckun, F. Uckun, 1998, Antimicrobial Agents and Chemotherapy.

Nucleoside conjugates. 15. Synthesis and biological activity of anti-HIV nucleoside conjugates of ether and thioether phospholipids.

C. K. Chu, C. West, K. Manouilov, 1996, Journal of medicinal chemistry.

D4T-5'-[p-bromophenyl methoxyalaninyl phosphate] as a potent and non-toxic anti-human immunodeficiency virus agent.

F. Uckun, T. Venkatachalam, R. Vig, 1998, Antiviral chemistry & chemotherapy.

Total Synthesis of 3'-O-Sialyl, 6'-O-Sulfo Lewisx, NeuAc.alpha.2.fwdarw.3(6-O-SO3Na)Ga1.beta.1.fwdarw.4(Fuc.alpha.1.fwdarw.3)GlcNAc.beta.-OMe: A Major Capping Group of GLYCAM-I

R. Jain, E. Chandrasekaran, K. Matta, 1994 .

Rational design and synthesis of phenethyl-5-bromopyridyl thiourea derivatives as potent non-nucleoside inhibitors of HIV reserve transcriptase.

F. Uckun, E. Sudbeck, T. Venkatachalam, 1998, Bioorganic & medicinal chemistry.

Nucleoside conjugates. 14. Synthesis and antitumor activity of 1-beta-D-arabinofuranosylcytosine conjugates of ether lipids with improved water solubility.

C. West, C. Hong, A. Nechaev, 1993, Journal of medicinal chemistry.