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Aleksey I. Gerasyuto, Ph.D. - Publications

Affiliations: 
2007 University of Wisconsin, Madison, Madison, WI 
Area:
Natural Product Synthesis
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22 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Narasimhan J, Letinski S, Jung SP, Gerasyuto A, Wang J, Arnold M, Chen G, Hedrick J, Dumble M, Ravichandran K, Levitz T, Chang C, Drennan CL, Stubbe J, Karp G, et al. Ribonucleotide reductase, a novel drug target for gonorrhea. Elife. 11. PMID 35137690 DOI: 10.7554/eLife.67447  0.591
2018 Gerasyuto AI, Arnold MA, Wang J, Chen G, Zhang X, Smith S, Woll MG, Baird J, Zhang N, Almstead NG, Narasimhan J, Peddi S, Dumble M, Sheedy J, Weetall M, et al. Correction to Discovery and Optimization of Indolyl-Containing 4-Hydroxy-2-pyridone Type II DNA Topoisomerase Inhibitors Active against Multidrug Resistant Gram-Negative Bacteria. Journal of Medicinal Chemistry. PMID 30351051 DOI: 10.1021/acs.jmedchem.8b01538  0.586
2018 Gerasyuto AI, Arnold MA, Wang J, Chen G, Zhang X, Smith S, Woll MG, Baird J, Zhang N, Almstead NG, Narasimhan J, Peddi S, Dumble M, Sheedy J, Weetall M, et al. Discovery and Optimization of Indolyl-Containing 4-Hydroxy-2-Pyridone Type II DNA Topoisomerase Inhibitors Active against Multi-Drug Resistant Gram-Negative Bacteria. Journal of Medicinal Chemistry. PMID 29727185 DOI: 10.1021/Acs.Jmedchem.8B00114  0.628
2017 Arnold MA, Gerasyuto AI, Wang J, Du W, Gorske YJK, Arasu T, Baird J, Almstead NG, Narasimhan J, Peddi S, Ginzburg O, Lue SW, Hedrick J, Sheedy J, Lagaud G, et al. 4-Hydroxy-2-pyridones: Discovery and evaluation of a novel class of antibacterial agents targeting DNA synthesis. Bioorganic & Medicinal Chemistry Letters. PMID 29032026 DOI: 10.1016/J.Bmcl.2017.10.006  0.671
2013 Gerasyuto AI, Ma ZX, Buchanan GS, Hsung RP. Establishing the concept of aza-[3 + 3] annulations using enones as a key expansion of this unified strategy in alkaloid synthesis. Beilstein Journal of Organic Chemistry. 9: 1170-8. PMID 23843910 DOI: 10.3762/Bjoc.9.131  0.779
2011 Buchanan GS, Dai H, Hsung RP, Gerasyuto AI, Scheinebeck CM. Asymmetric aza-[3+3] annulation in the synthesis of indolizidines: an unexpected reversal of regiochemistry. Organic Letters. 13: 4402-5. PMID 21786757 DOI: 10.1021/Ol2017438  0.756
2011 Ghosh SK, Wei Y, Gerasyuto AI, Feltenberger JB, Wang J, Hsung RP. ChemInform Abstract: A Cyclic Acetal Tethered Intramolecular Diels-Alder Cycloaddition. Studies Directed Toward a Total Synthesis of (.+-.)-Fusidilactone C. Cheminform. 42: no-no. DOI: 10.1002/chin.201131203  0.802
2010 Ghosh SK, Wei Y, Gerasyuto AI, Feltenberger JB, Wang J, Hsung RP. A cyclic acetal tethered intramolecular diels-alder cycloaddition. studies directed toward a total synthesis of (±)-fusidilactone C Heterocycles. 82: 1379-1409. DOI: 10.3987/Com-10-S(E)93  0.769
2008 Zhang Y, Gerasyuto AI, Long QA, Hsung RP. A General Approach to the Quinolizidine Alkaloids via an Intramolecular Aza-[3 + 3] Annulation. Synthesis of (±)-2-Deoxy-Lasubine II. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 2009: 237-240. PMID 19617925 DOI: 10.1055/S-0028-1087661  0.639
2007 Gerasyuto AI, Hsung RP. An intramolecular aza-[3+3] annulation approach to azaphenalene alkaloids. Total synthesis of myrrhine. The Journal of Organic Chemistry. 72: 2476-84. PMID 17338572 DOI: 10.1021/Jo062533H  0.707
2006 Gerasyuto AI, Hsung RP. Stereodivergent total syntheses of precoccinelline, hippodamine, coccinelline, and convergine. Organic Letters. 8: 4899-902. PMID 17020331 DOI: 10.1021/Ol0619359  0.602
2005 Sydorenko N, Zificsak CA, Gerasyuto AI, Hsung RP. Total syntheses of enantiomerically enriched R-(+)- and S-(-)-deplancheine. Organic & Biomolecular Chemistry. 3: 2140-4. PMID 15917902 DOI: 10.1039/B503862F  0.761
2005 Gerasyuto AI, Hsung RP, Sydorenko N, Slafer B. A formal [3 + 3] cycloaddition reaction. 5. An enantioselective intramolecular formal aza-[3 + 3] cycloaddition reaction promoted by chiral amine salts. The Journal of Organic Chemistry. 70: 4248-56. PMID 15903297 DOI: 10.1021/Jo050171S  0.82
2003 Shen HC, Wang J, Cole KP, McLaughlin MJ, Morgan CD, Douglas CJ, Hsung RP, Coverdale HA, Gerasyuto AI, Hahn JM, Liu J, Sklenicka HM, Wei LL, Zehnder LR, Zificsak CA. A formal [3 + 3] cycloaddition reaction. Improved reactivity using alpha,beta-unsaturated iminium salts and evidence for reversibility of 6pi-electron electrocyclic ring closure of 1-oxatrienes. The Journal of Organic Chemistry. 68: 1729-35. PMID 12608785 DOI: 10.1021/Jo020688T  0.706
2002 Sklenicka HM, Hsung RP, McLaughlin MJ, Wei LL, Gerasyuto AI, Brennessel WB. 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. Journal of the American Chemical Society. 124: 10435-42. PMID 12197745 DOI: 10.1021/Ja020698B  0.797
2002 Voskoboev NV, Gerasyuto AI, Zlotin SG. Synthesis of 3-methoxy-5-oxo-6-phenyl-5,6-dihydro-4H-isothiazolo[5,4-b] - 1,4-thiazine 7,7-dioxide, the first representative of a new heterocyclic system Russian Chemical Bulletin. 51: 191-192. DOI: 10.1023/A:1015002922937  0.443
2001 Wei LL, Hsung RP, Sklenicka HM, Gerasyuto AI. 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. Angewandte Chemie (International Ed. in English). 40: 1516-1518. PMID 29712373 DOI: 10.1002/1521-3773(20010417)40:8<1516::Aid-Anie1516>3.0.Co;2-V  0.812
2001 Wei LL, Hsung RP, Sklenicka HM, Gerasyuto AI. A Novel and Highly Stereoselective Intramolecular Formal Angewandte Chemie (International Ed. in English). 40: 1516-1518. PMID 11317320 DOI: 10.1002/1521-3773(20010417)40:8<1516::AID-ANIE1516>3.0.CO;2-V  0.803
2001 Gerasyuto AI, Zlotin SG, Semenov VV. 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 Synthesis. 300-304. DOI: 10.1055/S-2001-10820  0.489
2000 Sklenicka HM, Hsung RP, Wei LL, McLaughlin MJ, Gerasyuto AI, Degen SJ. Highly stereoselective formal Organic Letters. 2: 1161-4. PMID 10804579 DOI: 10.1021/Ol000049+  0.803
2000 Sklenicka HM, Hsung RP, Wei LL, McLaughlin MJ, Gerasyuto AI, Degen SJ. Highly stereoselective formal [3 + 3] cycloaddition reactions of chiral vinylogous amides with α,β-unsaturated iminiums Organic Letters. 2: 1161-1164.  0.768
1999 Zlotin SG, Gerasyuto AI. Methyl N-(benzylsulfonyl)oxamate as a probable intermediate in the synthesis of 4-hydroxy-5-phenyl-3(2H)-isothiazolone 1,1-dioxide from phenylmethanesulfamide and dimethyl oxalate in the presence of bases Russian Chemical Bulletin. 48: 396-398. DOI: 10.1007/Bf02494576  0.383
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