Ronald K. Russell
ScholarGPS® ID: 82502256738953
Affiliation History
Discipline
Chemistry
Top Specialties
Medicinal Chemistry | Chemical Synthesis | Receptor Modulator | Receptor Antagonist | Carboxylic Acid | Bacteria
Metrics Summary
Publication Count
58
Predicted Citations
1,236
Predicted h-index
16
Ranking
Publications and Citation History
Publications based on Top Specialties
Types of Publication
- Publications
- Books
- Patents
- NIH/NSF
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Synthesis of Mavatrep: A Potent Antagonist of Transient Receptor Potential Vanilloid-1 (journal article) Organic Process Research & Development, volume 19, issue 11, pages 1774-1783 (2015). |
Organic Process Research & Development, volume 18, issue 12, pages 1622-1629 (2014). |
Organic Process Research & Development, volume 18, issue 12, pages 1630-1640 (2014). |
Process Development for Scale-Up of a Novel 3,5-Substituted Thiazolidine-2,4-dione Compound as a Potent Inhibitor for Estrogen-Related Receptor 1 (journal article) Organic Process Research & Development, volume 18, issue 2, pages 321-330 (2014). |
Crystallization of a Cephalosporin and an ERR-1: Assembly of an Inexpensive Crystallization Platform (journal article) Crystal Growth & Design, volume 13, issue 11, pages 4635-4641 (2013). |
An Efficient Synthesis of 3-Substituted N -Glycoside Indoles Useful as Sodium-Dependent Glucose Transporter Inhibitors (journal article) Organic Process Research & Development, volume 16, issue 11, pages 1727-1732 (2012). |
Design and Characterization of Optimized Adenosine A2A /A1 Receptor Antagonists for the Treatment of Parkinson's Disease (journal article) Journal of Medicinal Chemistry, volume 55, issue 3, pages 1402-1417 (2012). |
Crystal Structure of (1-Cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-4-(oxo-\κO)-3-quinolinecarboxylato-κO3) difluoro-boron (journal article) Journal of Chemical Crystallography, volume 41, issue 6, pages 895-897 (2011). |
In Vivo Characterization of a Dual Adenosine A2A /A1 Receptor Antagonist in Animal Models of Parkinson’s Disease (journal article) Journal of Medicinal Chemistry, volume 53, issue 22, pages 8104-8115 (2010). |
ChemInform, volume 41, issue 38 (2010). |
Bioorganic & Medicinal Chemistry Letters, volume 20, issue 9, pages 2868-2871 (2010). |
Methylene amine substituted arylindenopyrimidines as potent adenosine A2A/A1 antagonists (journal article) Bioorganic & Medicinal Chemistry Letters, volume 20, issue 9, pages 2864-2867 (2010). |
Organic Preparations and Procedures International, volume 42, issue 2, pages 151-160 (2010). |
Regio- and diastereoselective ring-opening of (S)-(−)-2-(trifluoromethyl)oxirane with chiral 2,5-disubstituted tetrahydroquinolines in hexafluoro-2-propanol (journal article) Green Chemistry, volume 12, issue 9, pages 1548- (2010). |
Identification and Structure−Activity Relationships of Chromene-Derived Selective Estrogen Receptor Modulators for Treatment of Postmenopausal Symptoms (journal article) Journal of Medicinal Chemistry, volume 52, issue 23, pages 7544-7569 (2009). |
An Efficient Synthetic Process for Scale-Up Production of 4,5-Diamino-2-(trifluoromethyl)benzonitrile and 5-Bromo-3-(trifluoromethyl)benzene-1,2-diamine (journal article) Organic Process Research & Development, volume 13, issue 3, pages 652-655 (2009). |
Discovery and SAR of para-alkylthiophenoxyacetic acids as potent and selective PPARδ agonists (journal article) Bioorganic & Medicinal Chemistry Letters, volume 19, issue 4, pages 1101-1104 (2009). |
Organic Process Research & Development, volume 13, issue 1, pages 102-105 (2009). |
ChemInform Abstract: Scalable Synthesis of the VEGF‐R2 Kinase Inhibitor JNJ‐17029259 Using Ultrasound‐Mediated Addition of MeLi—CeCl3 to a Nitrile. (journal article) ChemInform, volume 39, issue 22 (2008). |
Organic Process Research & Development, volume 12, issue 3, pages 464-466 (2008). |