J. Ruiz-Caro

Computer-aided design of non-nucleoside inhibitors of HIV-1 reverse transcriptase.

Julian Tirado-Rives, William L Jorgensen, W. L. Jorgensen, 2006, Bioorganic & medicinal chemistry letters.

DIBALH mediated reduction of the acetal moiety on perhydrofuro[2,3-b]pyran derivatives.

J. Marco-Contelles, J. Ruiz-Caro, 2001, Carbohydrate research.

Bifunctional inhibition of human immunodeficiency virus type 1 reverse transcriptase: mechanism and proof-of-concept as a novel therapeutic design strategy.

Christopher M. Bailey, W. L. Jorgensen, K. Anderson, 2013, Journal of medicinal chemistry.

Selective transformations of differently functionalized 4-ethynyl-octa-1,7-dienes and 5-ethynyl-nona-1,8-dienes via intramolecular Pauson–Khand reaction: preparation of new and useful building blocks for the synthesis of angularly fused triquinanes

J. Marco-Contelles, L. Fensterbank, M. Malacria, 2002 .

Total synthesis of macroviracin D (BA-2836-4).

A. Fürstner, J. Ruiz-Caro, J. Młynarski, 2004, Chemistry.

Structure assignment, total synthesis, and evaluation of the phosphatase modulating activity of glucolipsin A.

H. Waldmann, H. Prinz, A. Fürstner, 2004, The Journal of organic chemistry.

Iridoids from Carbohydrates via Pauson-Khand Reaction: Synthesis of Advanced Highly Oxygenated Cyclopentane-Annulated Pyranosides from D-Glucal Derivatives.

J. Marco-Contelles, J. Ruiz-Caro, 1999, The Journal of organic chemistry.

Optimization of diarylamines as non-nucleoside inhibitors of HIV-1 reverse transcriptase.

William L Jorgensen, Christopher M. Bailey, W. L. Jorgensen, 2006, Bioorganic & medicinal chemistry letters.

Synthesis and transformations of new annulated pyranosides using the Pauson-Khand reaction.

J. Marco-Contelles, J. Ruiz-Caro, 2001, Carbohydrate research.