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Bryan J. Cowen, Ph.D.

Affiliations: 
Chemistry and Biochemistry University of Denver, Denver, CO, United States 
Website:
https://portfolio.du.edu/bcowen
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"Bryan Cowen"
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Parents

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Scott Joseph Miller grad student 2009 Yale
 (Enantioselective amine and phosphine-catalyzed reactions of allenic esters.)
David Y. Gin post-doc Memorial Sloan-Kettering
Derek S. Tan post-doc 2011-2012 Memorial Sloan Kettering Cancer Center
 (Postdoc with Prof. David Y. Gin)
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Publications

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Aretz CD, McPeak JE, Eaton GR, et al. (2018) Mechanism of SmI Reduction of 5-Bromo-6-oxo-6-phenylhexyl Methanesulfonate Studied by Spin Trapping with 2-Methyl-2-nitrosopropane. The Journal of Organic Chemistry
Ramann GA, Cowen BJ. (2016) Recent Advances in Metal-Free Quinoline Synthesis. Molecules (Basel, Switzerland). 21
Ramann GA, Cowen BJ. (2015) Quinoline synthesis by improved Skraup-Doebner-Von Miller reactions utilizing acrolein diethyl acetal Tetrahedron Letters. 56: 6436-6439
Saunders LB, Cowen BJ, Miller SJ. (2010) Pyridylalanine (Pal)-peptide catalyzed enantioselective allenoate additions to N-acyl imines proceed via an atypical "aza-Morita-Baylis-Hillman" mechanism. Organic Letters. 12: 4800-3
Cowen BJ, Miller SJ. (2009) Enantioselective catalysis and complexity generation from allenoates. Chemical Society Reviews. 38: 3102-16
Cowen BJ, Saunders LB, Miller SJ. (2009) Pyridylalanine (pal)-peptide catalyzed enantioselective allenoate additions to N-acyl imines. Journal of the American Chemical Society. 131: 6105-7
Cowen BJ, Saunders LB, Miller SJ. (2009) Enantioselective Allenoate Additions to Imines Synfacts. 2009: 682-682
Cowen BJ, Miller SJ. (2007) Enantioselective [3+2]-cycloadditions catalyzed by a protected, multifunctional phosphine-containing alpha-amino acid. Journal of the American Chemical Society. 129: 10988-9
Cowen BJ, Miller SJ. (2007) Enantioselective [3+2] Cycloadditions Synfacts. 2007: 1210-1210
Evans CA, Cowen BJ, Miller SJ. (2005) Diversity-generation from an allenoate-enone coupling: Syntheses of azepines and pyrimidones from common precursors Tetrahedron. 61: 6309-6314
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