H. Huynh

发表

ETX2514 is a broad-spectrum β-lactamase inhibitor for the treatment of drug-resistant Gram-negative bacteria including Acinetobacter baumannii

D. Ehmann, S. McLeod, Camilo Velez-Vega, 2017, Nature Microbiology.

Synthesis of Gal determinant epitopes, their glycomimetic variants, and trimeric clusters—relevance to tumor associated antigens and to discordant xenografts

M. Streiff, S. Hanessian, R. Oehrlein, 2001 .

β-Functionalization of Saturated Aza-Heterocycles Enabled by Organic Photoredox Catalysis.

David A. Nicewicz, B. Aquila, D. Nicewicz, 2021, ACS catalysis.

NMR Solution Structure of the Duplex Formed by Self-Pairing of α-L-Arabinopyranosyl-(4′2′)-(CGAATTCG)

M. Ebert, B. Jaun, A. Eschenmoser, 2002 .

Pentopyranosyl oligonucleotide systems: The β-D-xylopyranosyl-(4 → 2')-oligonucleotide system

A. Eschenmoser, R. Krishnamurthy, H. Huynh, 2002 .

Promiscuous Watson-Crick cross-pairing within the family of pentopyranosyl (4'-->2') oligonucleotides.

A. Eschenmoser, M. Stanek, R. Krishnamurthy, 1999, Organic letters.

Rational design of a new antibiotic class for drug-resistant infections

S. McLeod, A. Ferguson, G. Drusano, 2021, Nature.

Exploration of beta-turn scaffolding motifs as components of sialyl Le(X) mimetics and their relevance to P-selectin.

B. Ernst, H. Kolb, S. Hanessian, 1998, Bioorganic & medicinal chemistry letters.

Design and synthesis of sialyl Lex mimetics based on carbocyclic scaffolds derived from (−) quinic acid

B. Ernst, H. Kolb, S. Hanessian, 1997 .

Preparation of highly functionalized 1,5-disubstituted tetrazoles via palladium-catalyzed Suzuki coupling

E. Hennessy, V. Hoesch, Sudhir M. Hande, 2017 .

Discovery of Inhibitors of 4′-Phosphopantetheine Adenylyltransferase (PPAT) To Validate PPAT as a Target for Antibacterial Therapy

H. Ni, M. Johnstone, S. Lahiri, 2013, Antimicrobial Agents and Chemotherapy.

2,6-Diamino-5,8-diaza-7,9-dicarba-purine1

A. Eschenmoser, Bo Han, R. Krishnamurthy, 2003 .

2,6-Diamino-5,8-diaza-7,9-dicarba-purine.

A. Eschenmoser, Bo Han, R. Krishnamurthy, 2003, Organic letters.

Pentopyranosyl Oligonucleotide Systems. Communication No. 13

M. Ebert, B. Jaun, M. Beier, 2003 .

Discovery of bacterial NAD+-dependent DNA ligase inhibitors: optimization of antibacterial activity.

M. Gowravaram, Ce-Feng Liu, S. D. Mills, 2011, Bioorganic & medicinal chemistry letters.

Novel Bacterial NAD+-Dependent DNA Ligase Inhibitors with Broad-Spectrum Activity and Antibacterial Efficacy In Vivo

Kenneth D. Johnson, Wei Yang, A. Eakin, 2010, Antimicrobial Agents and Chemotherapy.

Discovery of bacterial NAD⁺-dependent DNA ligase inhibitors: improvements in clearance of adenosine series.

M. Gowravaram, T. O'Shea, S. D. Mills, 2012, Bioorganic & medicinal chemistry letters.

In Vivo Activity and Antibacterial Efficacy Ligase Inhibitors with Broad-Spectrum

Kenneth D. Johnson, A. Eakin, S. D. Mills, 2013 .

Novel Bacterial NAD +-dependent DNA Ligase Inhibitors with 3 Broad Spectrum Activity and Antibacterial Efficacy In Vivo 4 5 6 Running title : Novel Bacterial NAD +-dependent DNA Ligase Inhibitors 7 8 9

Kenneth D. Johnson, Wei Yang, A. Eakin, 2010 .

Discovery of AZD9833, a potent and orally bioavailable selective estrogen receptor degrader and antagonist.

O. Delpuech, J. Breed, J. Nissink, 2020, Journal of medicinal chemistry.

Enantioselective Synthesis and Profiling of Two Novel Diazabicyclooctanone β-Lactamase Inhibitors.

Yun Alelyunas, H. Xiong, T. Durand-Réville, 2014, ACS medicinal chemistry letters.

Building Bridges in a Series of Estrogen Receptor Degraders: An Application of Metathesis in Medicinal Chemistry.

J. Breed, J. Nissink, Paul R. J. Davey, 2019, ACS medicinal chemistry letters.

Formation of p-Alkoxybenzylidene Acetals on Solid Support and Generation of Functional Diversity with Carbohydrate Scaffolds

S. Hanessian, H. Huynh, 1999 .