Jonathan Richard Scheerer - Publications

Affiliations: 
2006 Harvard University, Cambridge, MA, United States 

25 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
2023 Scheerer JR, Leeth EB, Sprow JA. Synthesis of Guaipyridine Alkaloids Rupestine M and L by Cycloaddition/Cycloreversion of an Intermediate 1,4-Oxazinone. Synthesis. 55: 2319-2324. PMID 37691879 DOI: 10.1055/s-0042-1751413  0.304
2022 Pudner GL, Camp I, Scheerer JR. A Nonoxidative Sequence for the Preparation of 1,2-Diketone Derivatives Using Aldehyde and Organometallic Building Blocks. The Journal of Organic Chemistry. 87: 8213-8222. PMID 35613467 DOI: 10.1021/acs.joc.2c00439  0.356
2021 Carrillo Vallejo NA, Scheerer JR. Application of 1,4-Oxazinone Precursors to the Construction of Pyridine Derivatives by Tandem Intermolecular Cycloaddition/Cycloreversion. The Journal of Organic Chemistry. 86: 5863-5869. PMID 33797249 DOI: 10.1021/acs.joc.1c00288  0.44
2020 Angello NH, Wiley RE, Abelt CJ, Scheerer JR. Synthesis and Spectrophotometric Analysis of 1-Azafluorenone Derivatives. Molecules (Basel, Switzerland). 25. PMID 32722081 DOI: 10.3390/Molecules25153358  0.397
2020 Maisto SK, Leersnyder AP, Pudner GL, Scheerer JR. Synthesis of Pyrrolopyrazinones by Construction of the Pyrrole Ring onto an Intact Diketopiperazine. The Journal of Organic Chemistry. PMID 32602717 DOI: 10.1021/Acs.Joc.0C01263  0.521
2018 Angello NH, Wiley RE, Elmore TG, Perry RS, Scheerer JR. Domino Reaction Sequence for the Synthesis of [2.2.2]Diazabicycloalkenes and Base-Promoted Cycloreversion to 2-Pyridone Alkaloids. Organic Letters. PMID 30095269 DOI: 10.1021/Acs.Orglett.8B02145  0.465
2017 Williamson JB, Smith ER, Scheerer JR. A Merged Aldol Condensation, Alkene Isomerization, Cycloaddition/Cycloreversion Sequence Employing Oxazinone Intermediates for the Synthesis of Substituted Pyridines. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 28: 1170-1172. PMID 29398786 DOI: 10.1055/S-0036-1588729  0.501
2017 Perkins JC, Wang X, Pike RD, Scheerer JR. Further Investigation of the Intermolecular Diels-Alder Cycloaddition for the Synthesis of Bicyclo[2.2.2]diazaoctane Alkaloids. The Journal of Organic Chemistry. 82: 13656-13662. PMID 29172511 DOI: 10.1021/Acs.Joc.7B02403  0.572
2017 Kelley EW, Norman SG, Scheerer JR. Synthesis of monoalkylidene diketopiperazines and application to the synthesis of barettin. Organic & Biomolecular Chemistry. PMID 28980696 DOI: 10.1039/C7Ob02297B  0.532
2016 Nelli MR, Scheerer JR. Synthesis of Peramine, an Anti-insect Defensive Alkaloid Produced by Endophytic Fungi of Cool Season Grasses. Journal of Natural Products. PMID 26983087 DOI: 10.1021/Acs.Jnatprod.5B01089  0.554
2016 Robins JG, Kim KJ, Chinn AJ, Woo JS, Scheerer JR. Intermolecular Diels-Alder Cycloaddition for the Construction of Bicyclo[2.2.2]diazaoctane Structures: Formal Synthesis of Brevianamide B and Premalbrancheamide. The Journal of Organic Chemistry. PMID 26916112 DOI: 10.1021/Acs.Joc.5B02744  0.536
2015 Leibowitz MK, Winter ES, Scheerer JR. 3,4- and 3,5-Disubstituted 2-Pyridones Using an Intermolecular Cycloaddition / Cycloreversion Strategy: Toward the Synthesis of Aristopyridinone A. Tetrahedron Letters. 56: 6069-6072. PMID 26543258 DOI: 10.1016/J.Tetlet.2015.09.067  0.505
2015 Miller KE, Wright AJ, Olesen MK, Hovey MT, Scheerer JR. Stereoselective synthesis of (+)-loline alkaloid skeleton. The Journal of Organic Chemistry. 80: 1569-76. PMID 25611615 DOI: 10.1021/Jo502493E  0.484
2014 Margrey KA, Hazzard AD, Scheerer JR. Synthesis of 2-pyridones by cycloreversion of [2.2.2]- bicycloalkene diketopiperazines. Organic Letters. 16: 904-7. PMID 24476062 DOI: 10.1021/Ol403632T  0.537
2013 Laws SW, Scheerer JR. Enantioselective synthesis of (+)-malbrancheamide B. The Journal of Organic Chemistry. 78: 2422-9. PMID 23360221 DOI: 10.1021/Jo3026059  0.548
2013 Kwan EE, Scheerer JR, Evans DA. The stereochemical course of intramolecular Michael reactions. The Journal of Organic Chemistry. 78: 175-203. PMID 23186168 DOI: 10.1021/Jo302138Z  0.579
2012 Margrey KA, Chinn AJ, Laws SW, Pike RD, Scheerer JR. Efficient entry to the [2.2.2]-diazabicyclic ring system via diastereoselective domino reaction sequence. Organic Letters. 14: 2458-61. PMID 22571782 DOI: 10.1021/Ol3007056  0.548
2012 Eklund EJ, Pike RD, Scheerer JR. Synthesis of 1-aminopyrrolizidine alkaloid (-)-absouline by stereoselective aminoconjugate addition Tetrahedron Letters. 53: 4644-4647. DOI: 10.1016/J.Tetlet.2012.06.028  0.512
2011 Morris EN, Nenninger EK, Pike RD, Scheerer JR. Diels-Alder cycloaddition of chiral nonracemic 2,5-diketopiperazine dienes. Organic Letters. 13: 4430-3. PMID 21770431 DOI: 10.1021/Ol201768F  0.49
2011 Hovey MT, Eklund EJ, Pike RD, Mainkar AA, Scheerer JR. Synthesis of (±)-acetylnorloline via stereoselective tethered aminohydroxylation. Organic Letters. 13: 1246-9. PMID 21306134 DOI: 10.1021/Ol200155P  0.421
2008 Crawford JM, Thomas PM, Scheerer JR, Vagstad AL, Kelleher NL, Townsend CA. Deconstruction of iterative multidomain polyketide synthase function. Science (New York, N.Y.). 320: 243-6. PMID 18403714 DOI: 10.1126/Science.1154711  0.316
2007 Scheerer JR, Lawrence JF, Wang GC, Evans DA. Asymmetric synthesis of salvinorin A, a potent kappa opioid receptor agonist. Journal of the American Chemical Society. 129: 8968-9. PMID 17602636 DOI: 10.1021/Ja073590A  0.628
2007 Scheerer JR, Lawrence JF, Wang GC, Evans DA. Synthesis of Salvinorin A Synfacts. 2007: 1225-1225. DOI: 10.1055/S-2007-991305  0.628
2007 Scheerer JR, Lawrence JF, Wang GC, Evans DA. Asymmetric Synthesis of Salvinorin A (I), a Potent ϰ Opioid Receptor Agonist. Cheminform. 38. DOI: 10.1002/chin.200749186  0.404
2005 Evans DA, Scheerer JR. Polycyclic molecules from linear precursors: stereoselective synthesis of clavolonine and related complex structures. Angewandte Chemie (International Ed. in English). 44: 6038-42. PMID 16118819 DOI: 10.1002/Anie.200502296  0.484
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