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Synthesis of Nucleoside Phosphate and Phosphonate Prodrugs
Chemical reviews, 2014-09, Vol.114 (18), p.9154-9218
2014
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Structural insights into competitive antagonism in NMDA receptors
Neuron (Cambridge, Mass.), 2014-01, Vol.81 (2), p.366-378
2014
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Organometallic Enantiomeric Scaffolding: A Strategy for the Enantiocontrolled Construction of Regio- and Stereodivergent Trisubstituted Piperidines from a Common Precursor
Journal of the American Chemical Society, 2011-05, Vol.133 (19), p.7517-7527
2011
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Adenosine A2A receptor antagonism reverses inflammation-induced impairment of microglial process extension in a model of Parkinson's disease
Neurobiology of disease, 2014-07, Vol.67, p.191-202
2014
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Biased modulators of NMDA receptors control channel opening and ion selectivity
Nature chemical biology, 2020-02, Vol.16 (2), p.188
2020
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Ceramide synthase inhibition by fumonisin B1 causes accumulation of 1-deoxysphinganine: a novel category of bioactive 1-deoxysphingoid bases and 1-deoxydihydroceramides biosynthesized by mammalian cell lines and animals
The Journal of biological chemistry, 2009-02, Vol.284 (8), p.4786-4795
2009
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Synthesis and anti-HCV activity of a series of β-d-2′-deoxy-2′-dibromo nucleosides and their corresponding phosphoramidate prodrugs
Bioorganic & medicinal chemistry letters, 2017-12, Vol.27 (23), p.5296-5299
2017
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Design, Synthesis, and Structure–Activity Relationship of a Novel Series of GluN2C-Selective Potentiators
Journal of medicinal chemistry, 2014-03, Vol.57 (6), p.2334-2356
2014
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Novel Synthesis and Biological Evaluation of Enigmols as Therapeutic Agents for Treating Prostate Cancer
ACS medicinal chemistry letters, 2011-06, Vol.2 (6), p.438-443
2011
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Organometallic Enantiomeric Scaffolding. Sequential Semipinacol/1,5-“Michael-like” Reactions as a Strategic Approach to Bridgehead-Quaternary Center Aza[3.3.1]Bicyclics: Application to the Total Synthesis of (−)-Adaline
Journal of the American Chemical Society, 2009-01, Vol.131 (3), p.876-877
2009
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Correction to “Design, Synthesis, and Structure–Activity Relationship of a Novel Series of GluN2C-Selective Potentiators”
Journal of medicinal chemistry, 2015-03, Vol.58 (6), p.2862-2862
2015
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Novel Substitutions of 1-Alkoxy- and 1-Arylsulfonyloxy-η-Allylmolybdenum Complexes. A Case for η-Alkenyl Carbene Complexes as Intermediates
Organometallics, 2010-11, Vol.29 (21), p.5083-5097
2010
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Novel Substitutions of 1-Alkoxy- and 1-Arylsulfonyloxy-η3-allylmolybdenum Complexes. A Case for η1-Alkenyl Carbene Complexes as Intermediates
Organometallics, 2010-11, Vol.29 (21), p.5083-5097
2010
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ChemInform Abstract: Synthesis of Nucleoside Phosphate and Phosphonate Prodrugs
ChemInform, 2014-11, Vol.45 (45), p.no-no
2014
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Ceramide Synthase Inhibition by Fumonisin B1 Causes Accumulation of 1-Deoxysphinganine
The Journal of biological chemistry, 2009-02, Vol.284 (8), p.4786-4795
2009
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ChemInform Abstract: Organometallic Enantiomeric Scaffolding: A Strategy for the Enantiocontrolled Construction of Regio- and Stereodivergent Trisubstituted Piperidines from a Common Precursor
ChemInform, 2011-10, Vol.42 (41), p.no-no
2011
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Novel Substitutions of 1-Alkoxy- and 1-Arylsulfonyloxy-η 3 -allylmolybdenum Complexes. A Case for η 1 -Alkenyl Carbene Complexes as Intermediates
Organometallics, 2010-11, Vol.29 (21), p.5083-5097
2010
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Transition Metal‐Catalyzed Desulfitative Coupling of Thioorganic Compounds with Boronic Acids
Boronic Acids, 2011, p.363-391
2011
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Ceramide synthase inhibition by fumonisin B₁ causes accumulation of 1-deoxy-sphinganine: A novel category of bioactive 1-deoxy-sphingoid bases and 1-deoxy-dihydroceramides biosynthesized by mammalian cell lines and animals
The Journal of biological chemistry, 2009, Vol.284 (8), p.4786-4795
2009
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Toward Chemoselective Bioconjugative Desulfitative Catalysis
Advances in Organometallic Chemistry and Catalysis, 2013, p.295-303
2013
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