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Rhonan Ford

Observed name: Rhonan L. Ford
OpenAlex ID: A5081875340
Cell-permeable succinate prodrugs bypass mitochondrial complex I deficiency
2016 · Johannes K. Ehinger, Sarah Piel, et al. · Nature Communications · 142
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Experimental Measurement of Noncovalent Interactions Between Halogens and Aromatic Rings
2004 · Harry Adams, Scott L. Cockroft, et al. · ChemBioChem · 60
Cathepsin C Inhibitors: Property Optimization and Identification of a Clinical Candidate
2014 · Mark Furber, Anna-Karin Tiden, et al. · Journal of Medicinal Chemistry · 54
Structure-driven HtL: Design and synthesis of novel aminoindazole inhibitors of c-Jun N-terminal kinase activity
2005 · Michael J. Stocks, Simon Barber, et al. · Bioorganic & Medicinal Chemistry Letters · 48
The discovery of AZD9164, a novel muscarinic M3 antagonist
2011 · Antonio Mete, Keith Bowers, et al. · Bioorganic & Medicinal Chemistry Letters · 21
An Approach to the Tricyclic Lactone Core of Brasoside and Related Natural Products
2004 · Jeremy Robertson, Morgan Ménard, et al. · Synlett · 12
The design of a novel series of muscarinic receptor antagonists leading to AZD8683, a potential inhaled treatment for COPD
2013 · Antonio Mete, Keith Bowers, et al. · Bioorganic & Medicinal Chemistry Letters · 10
Conjugate addition of organocopper reagents to γ-alkoxybutenolides and application to the synthesis of non-racemic alkyl cyclopentenones
2004 · Jeremy Robertson, Morgan Ménard, et al. · Organic & Biomolecular Chemistry · 10
A synthesis of (−)-ebelactones A and B
2010 · John P. Cooksey, Rhonan Ford, et al. · Tetrahedron · 7
Prolyl Isomerases -Old Proteins as New Therapeutic Targets
2015 · Carol Austin, John B. Davis, et al. · 2
Structure‐Driven HtL: Design and Synthesis of Novel Aminoindazole Inhibitors of c‐Jun N‐Terminal Kinase Activity.
2005 · Michael J. Stocks, Simon Barber, et al. · ChemInform · 1
Conjugate Addition of Organocopper Reagents to γ‐Alkoxybutenolides and Application to the Synthesis of Non‐racemic Alkyl Cyclopentenones.
2005 · Jeremy Robertson, Morgan Menard, et al. · ChemInform
Works count: 12
Citation count: 367
H-index: 8
I10-index: 8
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