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Atom Transfer Reactions of TMM Diyls Directed toward the Synthesis of Rudmollin

Organic letters, 2000-08, Vol.2 (16), p.2531-2534

2000

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Total synthesis of psorospermin

Tetrahedron letters, 2005-01, Vol.46 (5), p.827-829

2005

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Potent, Orally Active Corticotropin-Releasing Factor Receptor-1 Antagonists Containing a Tricyclic Pyrrolopyridine or Pyrazolopyridine Core

Journal of medicinal chemistry, 2005-06, Vol.48 (12), p.4100-4110

2005

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Nickel(0)-catalyzed coupling of vinylzirconiums to α-bromo-α,α-difluoro esters. Convenient generation of a functionalized allyldifluoro moiety

Tetrahedron letters, 2000-02, Vol.41 (6), p.791-794

2000

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Clinical development of CX-3543, a novel multi-targeting antitumor agent

Journal of clinical oncology, 2005-06, Vol.23 (16_suppl), p.3206-3206

2005

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A modified electrochemical approach to diazenes: Electrochemistry in organic synthesis

Electrochimica acta, 1997, Vol.42 (13-14), p.2201-2203

1997

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Organometallic nucleophilic ring-opening of endo peroxides

Tetrahedron letters, 1996-09, Vol.37 (37), p.6635-6638

1996

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A modified electrochemical approach to diazenes

Electrochimica acta, 1997, Vol.42 (13), p.2201-2203

1997

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An Improved Workup for Samarium (II) Iodide Reactions

Synthetic communications, 1997-03, Vol.27 (5), p.837-840

1997

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ChemInform Abstract: An Improved Workup for Samarium(II) Iodide Reactions

ChemInform, 1997-06, Vol.28 (26), p.no-no

1997

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ChemInform Abstract: Organometallic Nucleophilic Ring-Opening of endo Peroxides

ChemInform, 1996-12, Vol.27 (52), p.no-no

1996

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Inhibition of RNA Polymerase I as a Therapeutic Strategy to Promote Cancer-Specific Activation of p53

Cancer cell, 2012-07, Vol.22 (1), p.51-65

2012

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CX-4945, an orally bioavailable selective inhibitor of protein kinase CK2, inhibits prosurvival and angiogenic signaling and exhibits antitumor efficacy

Cancer research (Chicago, Ill.), 2010-12, Vol.70 (24), p.10288-10298

2010

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Autism risk in small- and large-for-gestational-age infants

American journal of obstetrics and gynecology, 2012-04, Vol.206 (4), p.314.e1-314.e9

2012

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Discovery and SAR of 5-(3-Chlorophenylamino)benzo[c][2,6]naphthyridine-8-carboxylic Acid (CX-4945), the First Clinical Stage Inhibitor of Protein Kinase CK2 for the Treatment of Cancer

Journal of medicinal chemistry, 2011-01, Vol.54 (2), p.635-654

2011

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Pre-clinical characterization of CX-4945, a potent and selective small molecule inhibitor of CK2 for the treatment of cancer

Molecular and cellular biochemistry, 2011-10, Vol.356 (1-2), p.37-43

2011

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Discovery of CX-5461, the First Direct and Selective Inhibitor of RNA Polymerase I, for Cancer Therapeutics

ACS medicinal chemistry letters, 2012-07, Vol.3 (7), p.602-606

2012

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Discovery of CX-6258. A Potent, Selective, and Orally Efficacious pan-Pim Kinases Inhibitor

ACS medicinal chemistry letters, 2012-02, Vol.3 (2), p.135-139

2012

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A Facile Synthesis of 5-Halopyrimidine-4-Carboxylic Acid Esters via a Minisci Reaction

Synlett, 2012-02, Vol.23 (3), p.443-447

2012

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Techno-Economic Analysis of Material Costs for Emerging Flow Batteries

REWAS 2022: Developing Tomorrow’s Technical Cycles (Volume I), p.449-460

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Novel potent pyrimido[4,5- c]quinoline inhibitors of protein kinase CK2: SAR and preliminary assessment of their analgesic and anti-viral properties

Bioorganic & medicinal chemistry letters, 2011-03, Vol.21 (6), p.1687-1691

2011

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Synthesis and SAR of inhibitors of protein kinase CK2: Novel tricyclic quinoline analogs

Bioorganic & medicinal chemistry letters, 2012-01, Vol.22 (1), p.45-48

2012

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Facile and efficient generation of quinolone amides from esters using aluminum chloride

Tetrahedron letters, 2011-03, Vol.52 (10), p.1096-1100

2011

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CEUS in gunshot wound of the liver – first experience in military mission

Ultraschall in der Medizin, 2016-08, Vol.37 (S 01)

2016

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Retrospektive Auswertung der von 2005 bis 2012 an einem offenen 1.0 Tesla MRT-Tomographen durchgeführten Federhaken-Markierungen der Mammae

RöFo : Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebende Verfahren, 2014, Vol.186 (S 01)

2014

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Atom Transfer Reactions of TMM Diyls Directed toward the Synthesis of Rudmollin

Total synthesis of psorospermin

Potent, Orally Active Corticotropin-Releasing Factor Receptor-1 Antagonists Containing a Tricyclic Pyrrolopyridine or Pyrazolopyridine Core

Nickel(0)-catalyzed coupling of vinylzirconiums to α-bromo-α,α-difluoro esters. Convenient generation of a functionalized allyldifluoro moiety

Clinical development of CX-3543, a novel multi-targeting antitumor agent

A modified electrochemical approach to diazenes: Electrochemistry in organic synthesis

Organometallic nucleophilic ring-opening of endo peroxides

A modified electrochemical approach to diazenes

An Improved Workup for Samarium (II) Iodide Reactions

ChemInform Abstract: An Improved Workup for Samarium(II) Iodide Reactions

ChemInform Abstract: Organometallic Nucleophilic Ring-Opening of endo Peroxides

Inhibition of RNA Polymerase I as a Therapeutic Strategy to Promote Cancer-Specific Activation of p53

CX-4945, an orally bioavailable selective inhibitor of protein kinase CK2, inhibits prosurvival and angiogenic signaling and exhibits antitumor efficacy

Autism risk in small- and large-for-gestational-age infants

Discovery and SAR of 5-(3-Chlorophenylamino)benzo[c][2,6]naphthyridine-8-carboxylic Acid (CX-4945), the First Clinical Stage Inhibitor of Protein Kinase CK2 for the Treatment of Cancer

Pre-clinical characterization of CX-4945, a potent and selective small molecule inhibitor of CK2 for the treatment of cancer

Discovery of CX-5461, the First Direct and Selective Inhibitor of RNA Polymerase I, for Cancer Therapeutics

Discovery of CX-6258. A Potent, Selective, and Orally Efficacious pan-Pim Kinases Inhibitor

A Facile Synthesis of 5-Halopyrimidine-4-Carboxylic Acid Esters via a Minisci Reaction

Techno-Economic Analysis of Material Costs for Emerging Flow Batteries

Novel potent pyrimido[4,5- c]quinoline inhibitors of protein kinase CK2: SAR and preliminary assessment of their analgesic and anti-viral properties

Synthesis and SAR of inhibitors of protein kinase CK2: Novel tricyclic quinoline analogs

Facile and efficient generation of quinolone amides from esters using aluminum chloride

CEUS in gunshot wound of the liver – first experience in military mission

Retrospektive Auswertung der von 2005 bis 2012 an einem offenen 1.0 Tesla MRT-Tomographen durchgeführten Federhaken-Markierungen der Mammae

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