A. Gerasyuto

发表

4-Hydroxy-2-pyridones: Discovery and evaluation of a novel class of antibacterial agents targeting DNA synthesis.

J. Narasimhan, A. Branstrom, Josephine Sheedy, 2017, Bioorganic & medicinal chemistry letters.

Asymmetric aza-[3+3] annulation in the synthesis of indolizidines: an unexpected reversal of regiochemistry.

R. Hsung, Casi M. Scheinebeck, A. Gerasyuto, 2011, Organic letters.

A Novel and Highly Stereoselective Intramolecular Formal [3+3] Cycloaddition Reaction of Vinylogous Amides Tethered with α,β-Unsaturated Aldehydes: A Formal Total Synthesis of (+)-Gephyrotoxin.

R. Hsung, A. Gerasyuto, Lin-Li Wei, 2001, Angewandte Chemie.

A Formal [3 + 3] Cycloaddition Reaction. Improved Reactivity Using α,β-Unsaturated Iminium Salts and Evidence for Reversibility of 6π-Electron Electrocyclic Ring Closure of 1-Oxatrienes

R. Hsung, J. Liu, Hong C Shen, 2003 .

A formal [3 + 3] cycloaddition reaction. 5. An enantioselective intramolecular formal aza-[3 + 3] cycloaddition reaction promoted by chiral amine salts.

R. Hsung, B. Slafer, N. Sydorenko, 2005, The Journal of organic chemistry.

Stereoselective formal [3 + 3] cycloaddition approach to cis-1-azadecalins and synthesis of (-)-4a,8a-diepi-pumiliotoxin C. evidence for the first highly stereoselective 6pi-electron electrocyclic ring closures of 1-azatrienes.

R. Hsung, M. McLaughlin, A. Gerasyuto, 2002, Journal of the American Chemical Society.

Highly Stereoselective Formal [3 + 3] Cycloaddition Reactions of Chiral Vinylogous Amides with α,β-Unsaturated Iminiums

R. Hsung, M. McLaughlin, A. Gerasyuto, 2000 .

Total syntheses of enantiomerically enriched R-(+)- and S-(-)-deplancheine.

R. Hsung, N. Sydorenko, A. Gerasyuto, 2005, Organic & biomolecular chemistry.

Establishing the concept of aza-[3 + 3] annulations using enones as a key expansion of this unified strategy in alkaloid synthesis

R. Hsung, Zhi-Xiong Ma, A. Gerasyuto, 2013, Beilstein journal of organic chemistry.

A Novel and Highly Stereoselective Intramolecular Formal [3 + 3] Cycloaddition Reaction of Vinylogous Amides Tethered with α,β-Unsaturated Aldehydes: A Formal Total Synthesis of (+)-Gephyrotoxin.

R. Hsung, A. Gerasyuto, Lin-Li Wei, 2001 .

Stereodivergent total syntheses of precoccinelline, hippodamine, coccinelline, and convergine.

R. Hsung, A. Gerasyuto, 2006, Organic letters.

Ribonucleotide reductase, a novel target for gonorrhea

J. Stubbe, J. Narasimhan, A. Branstrom, 2020, bioRxiv.

Synthesis of 2,3-Dihydrobenzothiazol-1,1-dioxide and 2,3-Dihydro-1,4-benzothiazin-3-one Nitroderivatives from 2,4-Di- and 2,4,6-Trinitrobenzamides

S. Zlotin, V. Semenov, A. Gerasyuto, 2001 .

Identification of Potent Paracaspase MALT1 Inhibitors for Hematological Malignancies

V. Feher, M. Lawrenz, Sayantan Mondal, 2020 .

An intramolecular aza-[3+3] annulation approach to azaphenalene alkaloids. Total synthesis of myrrhine.

R. Hsung, A. Gerasyuto, 2007, The Journal of organic chemistry.

Potent Antimalarials with Development Potential Identified by Structure-Guided Computational Optimization of a Pyrrole-Based Dihydroorotate Dehydrogenase Inhibitor Series.

David M. Shackleford, E. Winzeler, P. Rathod, 2021, Journal of medicinal chemistry.

A Cyclic Acetal Tethered Intramolecular Diels—Alder Cycloaddition. Studies Directed Toward a Total Synthesis of (.+-.)-Fusidilactone C.

R. Hsung, S. Ghosh, Yonggang Wei, 2011 .

Characterization of Potent Paracaspase MALT1 Inhibitors for Hematological Malignancies

V. Feher, M. Lawrenz, M. Ye, 2021, Blood.