E. Elhalem

发表

Exploring the influence of indololactone structure on selectivity for binding to the C1 domains of PKCα, PKCε, and RasGRP.

Megan L. Peach, P. Blumberg, M. Peach, 2017, Bioorganic & medicinal chemistry.

Structural determinants of efficacy at A3 adenosine receptors: modification of the ribose moiety.

K. Jacobson, Zhang-Guo Gao, H. Moon, 2004, Biochemical pharmacology.

Proline-coated gold nanoparticles as a highly efficient nanocatalyst for the enantioselective direct aldol reaction in water

N. Khiar, I. Fernández, E. Elhalem, 2013 .

NMR study on the stabilization and chiral discrimination of sulforaphane enantiomers and analogues by cyclodextrins.

J. M. Benito, N. Khiar, I. Fernández, 2017, Carbohydrate polymers.

Studies on the diastereoselective oxidation of 1-thio-β-D-glucopyranosides: synthesis of the usually less favoured R(S) sulfoxide as a single diastereoisomer.

E. Álvarez, N. Khiar, I. Fernández, 2015, Organic & biomolecular chemistry.

Design, Synthesis and Characterization of Novel sn-1 Heterocyclic DAGlactones as PKCe Activators

M. Kazanietz, M. Peach, L. Pearce, 2020 .

Design, Synthesis and Characterization of Novel sn-1 Heterocyclic DAG- lactones as PKCe Activators

M. Kazanietz, M. Peach, Mariana Cooke, 2020 .

Synthesis and biological evaluation of N-thia-carba-thymidine as an antiherpetic agent

E. Damonte, Juan B Rodriguez, E. Elhalem, 2010 .

Design, synthesis, and biological evaluation of aryloxyethyl thiocyanate derivatives against Trypanosoma cruzi.

R. Docampo, Juan B Rodriguez, S. Szajnman, 2002, Journal of medicinal chemistry.

Design and synthesis of aryloxyethyl thiocyanate derivatives as potent inhibitors of Trypanosoma cruzi proliferation.

R. Docampo, S. Szajnman, E. Elhalem, 2000, Journal of medicinal chemistry.

Synthesis of Conformationally Locked Carbocyclic Nucleosides Built on a Thiabicyclo[3.1.0]hexane System as a Pseudosugar Surrogate

Juan B Rodriguez, E. Elhalem, M. Comin, 2006 .

Sulforaphane homologues: Enantiodivergent synthesis of both enantiomers, activation of the Nrf2 transcription factor and selective cytotoxic activity.

M. López-Lázaro, N. Khiar, I. Fernández, 2014, European journal of medicinal chemistry.

Synthetic studies toward the preparation of (4R,5R)-(−)-3-[(benzyloxy)methyl]-4,5-O-isopropylidene-cyclopenten-2-one: an important synthetic intermediate for carbanucleosides

Juan B Rodriguez, E. Elhalem, M. Comin, 2005 .

Cerium ammonium nitrate: a new catalyst for regioselective protection of glycols

Juan B Rodriguez, E. Elhalem, M. Comin, 2004 .

Design, Synthesis, and Characterization of Novel sn-1 Heterocyclic DAG-Lactones as PKC Activators.

Megan L. Peach, M. Kazanietz, M. Peach, 2021, Journal of medicinal chemistry.