A. Goldblum

Toxicity modulation, resistance enzyme evasion, and A-site X-ray structure of broad-spectrum antibacterial neomycin analogs.

L. A. Feeney, J. Kondo, J. P. Maianti, 2014, ACS chemical biology.

A multivalent approach to the design and discovery of orally efficacious 5-HT4 receptor agonists.

S. D. Turner, J. Shaw, S. Choi, 2009, Journal of medicinal chemistry.

Toward Overcoming Staphylococcus aureus Aminoglycoside Resistance Mechanisms with a Functionally Designed Neomycin Analogue.

L. A. Feeney, J. P. Maianti, S. Hanessian, 2011, ACS medicinal chemistry letters.

Discovery, oral pharmacokinetics and in vivo efficacy of a highly selective 5-HT4 receptor agonist: clinical compound TD-2749.

J. Shaw, S. Choi, R. Vickery, 2012, Bioorganic & medicinal chemistry letters.

Discovery, oral pharmacokinetics and in vivo efficacy of velusetrag, a highly selective 5-HT(4) receptor agonist that has achieved proof-of-concept in patients with chronic idiopathic constipation.

S. D. Turner, J. Shaw, S. Choi, 2012, Bioorganic & medicinal chemistry letters.

Stereocontrolled Synthesis of (±)-Grandisol

Derek A. Fischer, J. Read de Alaniz, C. Switzer, 2022, Synthesis.

Synthesis and Microbiological Evaluation of Novel Tetracyclic Fluoroquinolones

T. Poel, H. Moser, A. Wagman, 2017, ChemMedChem.

Synthesis and Spectrum of the Neoglycoside ACHN-490

L. A. Feeney, Rowena D. Matias, H. Moser, 2010, Antimicrobial Agents and Chemotherapy.