Barry M. Twenter

发表

Total synthesis of (±)-phomoidride D: A 22 year odyssey

Ping Dong, Jon T. Njardarson, Joyce C. Leung, 2018 .

Regiocontrolled synthesis and HIV inhibitory activity of unsymmetrical binaphthoquinone and trimeric naphthoquinone derivatives of conocurvone.

Barry M. Twenter, Y. Pommier, J. Harwood, 2006, Bioorganic & Medicinal Chemistry.

A 3-(4-Nitronaphthen-1-yl) amino-benzoate analog as a Bifunctional AKR1C3 Inhibitor with AR Antagonist Activity: Head to Head Comparison with Other Advanced AKR1C3 Targeted Therapeutics

Barry M. Twenter, J. Winkler, A. Adeniji, 2019 .

A 3-(4-nitronaphthen-1-yl) amino-benzoate analog as a bifunctional AKR1C3 inhibitor and AR antagonist: Head to head comparison with other advanced AKR1C3 targeted therapeutics

Barry M. Twenter, J. Winkler, A. Adeniji, 2019, The Journal of Steroid Biochemistry and Molecular Biology.

Discovery of substituted 3-(phenylamino)benzoic acids as potent and selective inhibitors of type 5 17β-hydroxysteroid dehydrogenase (AKR1C3).

Barry M. Twenter, J. Winkler, A. Adeniji, 2011, Bioorganic & medicinal chemistry letters.

Toward the synthesis of phomoidride D.

Aaron A. Bedermann, Graham K. Murphy, Barry M. Twenter, 2013, The Journal of organic chemistry.

Total Synthesis of (±)-Phomoidride D.

Aaron A. Bedermann, Joyce C. Leung, Graham K. Murphy, 2018, Angewandte Chemie.

Wharton-fragmentation-based approach to the carbocyclic core of the phomoidrides.

Aaron A. Bedermann, Graham K. Murphy, Barry M. Twenter, 2012, Organic letters.

Synthesis of Substituted Phenazines via Palladium-Catalyzed Aryl Ligation.

Barry M. Twenter, J. Winkler, T. Gendrineau, 2012 .

A NEW APPROACH TO THE SYNTHESIS OF SUBSTITUTED PHENAZINES VIA PALLADIUM-CATALYZED ARYL LIGATIONi.

Barry M. Twenter, J. Winkler, T. Gendrineau, 2012, Heterocycles.

Development of potent and selective inhibitors of aldo-keto reductase 1C3 (type 5 17β-hydroxysteroid dehydrogenase) based on N-phenyl-aminobenzoates and their structure-activity relationships.

Barry M. Twenter, J. Winkler, A. Adeniji, 2012, Journal of medicinal chemistry.

Crystal structures of AKR1C3 containing an N-(aryl)amino-benzoate inhibitor and a bifunctional AKR1C3 inhibitor and androgen receptor antagonist. Therapeutic leads for castrate resistant prostate cancer.

Barry M. Twenter, J. Winkler, D. Christianson, 2012, Bioorganic & medicinal chemistry letters.