Shawn Branum

Biochemistry, Genetics and Molecular Biology · Life Sciences

9h-index236citations16works0.02yr avg
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Research Topics

Adenosine and Purinergic Signaling(4), Bioactive Compounds and Antitumor Agents(3), Synthesis and Reactions of Organic Compounds(3), Carbohydrate Chemistry and Synthesis(2), Chemical Synthesis and Analysis(2)

Publications16 total

CCDC 931421: Experimental Crystal Structure Determination
The Cambridge Structural Database·2015Open Access
Lab-Scale Preparation of a Novel Cyclopenta[b]furan Chemokine Receptor Antagonist
Organic Process Research & Development·2014· 10 cited
Lab-Scale Preparation of a Novel Carbocyclic Chemokine Receptor Antagonist
Organic Process Research & Development·2014· 7 cited
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
Organic Process Research & Development·2014· 14 cited
An Efficient Synthesis of 3-Substituted <i>N</i>-Glycoside Indoles Useful as Sodium-Dependent Glucose Transporter Inhibitors
Organic Process Research & Development·2012· 9 cited
Design and Characterization of Optimized Adenosine A<sub>2A</sub>/A<sub>1</sub> Receptor Antagonists for the Treatment of Parkinson's Disease
Journal of Medicinal Chemistry·2012· 46 citedOpen Access
In Vivo Characterization of a Dual Adenosine A<sub>2A</sub>/A<sub>1</sub> Receptor Antagonist in Animal Models of Parkinson’s Disease
Journal of Medicinal Chemistry·2010· 54 citedOpen Access
Methylene amine substituted arylindenopyrimidines as potent adenosine A2A/A1 antagonists
Bioorganic & Medicinal Chemistry Letters·2010· 24 citedOpen Access
Optimization of arylindenopyrimidines as potent adenosine A2A/A1 antagonists
Bioorganic & Medicinal Chemistry Letters·2010· 12 citedOpen Access
Regio- and diastereoselective ring-opening of (S)-(−)-2-(trifluoromethyl)oxirane with chiral 2,5-disubstituted tetrahydroquinolines in hexafluoro-2-propanol
Green Chemistry·2010· 3 cited
Synthesis of Tetracyclic Heterocompounds as Selective Estrogen Receptor Modulators. Part 2. Process Improvement for Scale-Up of 2,5,8-Substituted 11,12-Dihydro-5<i>H</i>-6,13-dioxabenzo[3,4]cyclohepta-[1,2-<i>a</i>]naphthalene Derivatives
Organic Process Research & Development·2007· 7 cited
Synthesis of Tetracyclic Heterocompounds as Selective Estrogen Receptor Modulators. Part 2. Process Improvement for Scale-Up Of 2,5,8-Substituted 11,12-Dihydro-5<i>H</i>-6,13-dioxabenzo[3,4]cyclohepta-[1,2-<i>a</i>]naphthalene Derivatives
Organic Process Research & Development·2007· 8 cited
Synthesis of Tetracyclic Heterocompounds as Selective Estrogen Receptor Modulators. Part 1. Process Development for Scale-up of 2,5,8-Substituted 5,11-Dihydrochromeno[4,3-<i>c</i>]chromene Derivatives
Organic Process Research & Development·2007· 11 cited
Development of a Scalable Synthetic Process for Selective Bromination of 4-Methyl-3,7-Substituted Coumarins
Organic Process Research & Development·2006· 12 cited
An Efficient Process for Synthesis of 3-(<i>R</i>)-3-(2,3-Dihydrobenzofuran-5-yl)- 1,2,3,4-tetrahydropyrrolo[3,4-<i>b</i>]quinolin-9-one
Organic Process Research & Development·2005· 16 cited
The synthesis of (9S)-9-alkyl-9-hydroxyerythromycin A derivatives and their ketolides
Tetrahedron Letters·2005· 3 cited

Frequent Co-authors

Ronald K. Russell(15), Scott Youells(8), Derek A. Beauchamp(8), Zhihua Sui(8), Kenneth M. Wells(6), Xun Li(6), Michael Reuman(6), Sandra Damon(5), Brian C. Shook(4), Stefanie Rassnick(4), Lori Westover(4), Devraj Chakravarty(4), Kenneth J. Rhodes(4), Paul Jackson(4), Christopher A. Teleha(4), William V. Murray(4), Nareshkumar Jain(4), D.W.R. Hall(3), Kenneth C. Rupert(3), Geoffrey R. Heintzelman(3)