Eddie L. Myers - Publications

Affiliations: 
2006-2009 University of Wisconsin, Madison, Madison, WI 

29 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 Aiken SG, Bateman JM, Liao HH, Fawcett A, Bootwicha T, Vincetti P, Myers EL, Noble A, Aggarwal VK. Iterative synthesis of 1,3-polyboronic esters with high stereocontrol and application to the synthesis of bahamaolide A. Nature Chemistry. PMID 36424454 DOI: 10.1038/s41557-022-01087-9  0.352
2019 Myers EL, Palte MJ, Raines RT. Catalysis of Hydrogen-Deuterium Exchange Reactions by 4-Substituted Proline Derivatives. The Journal of Organic Chemistry. PMID 30602119 DOI: 10.1021/Acs.Joc.8B02644  0.59
2018 Mykura RC, Veth S, Varela A, Dewis L, Farndon JJ, Myers EL, Aggarwal VK. Investigation of the Deprotonative Generation and Borylation of Diamine-Ligated α-Lithiated Carbamates and Benzoates by in situ IR spectroscopy. Journal of the American Chemical Society. PMID 30260635 DOI: 10.1021/Jacs.8B06871  0.419
2018 Armstrong RJ, Nandakumar M, Dias RMP, Noble A, Myers EL, Aggarwal VK. Enantiodivergent Synthesis of Allenes by Point to Axial Chirality Transfer. Angewandte Chemie (International Ed. in English). PMID 29719111 DOI: 10.1002/Anie.201804446  0.412
2018 Noble A, Mega RS, Pflästerer D, Myers EL, Aggarwal VK. Visible-Light-Mediated Decarboxylative Radical Additions to Vinyl Boronic Esters: Rapid Access to γ-Amino Boronic Esters. Angewandte Chemie (International Ed. in English). PMID 29316095 DOI: 10.1002/Anie.201712186  0.409
2017 Lorenzo P, Butts CP, Myers EL, Aggarwal VK. The Story behind "Synergy of Synthesis, Computation, and NMR Reveals Correct Baulamycin Structures". Biochemistry. PMID 29125284 DOI: 10.1021/Acs.Biochem.7B00994  0.315
2017 Bootwicha T, Feilner JM, Myers EL, Aggarwal VK. Iterative assembly line synthesis of polypropionates with full stereocontrol. Nature Chemistry. 9: 896-902. PMID 28837173 DOI: 10.1038/Nchem.2757  0.34
2017 Casoni G, Kucukdisli M, Fordham JM, Burns M, Myers EL, Aggarwal VK. α-Sulfinyl Benzoates as Precursors to Li and Mg Carbenoids for the Stereoselective Iterative Homologation of Boronic Esters. Journal of the American Chemical Society. PMID 28812893 DOI: 10.1021/Jacs.7B05457  0.384
2017 Wu J, Lorenzo P, Zhong S, Ali M, Butts CP, Myers EL, Aggarwal VK. Synergy of synthesis, computation and NMR reveals correct baulamycin structures. Nature. 547: 436-440. PMID 28748934 DOI: 10.1038/Nature23265  0.328
2017 Smith JR, Collins BSL, Hesse MJ, Graham MA, Myers EL, Aggarwal VK. Enantioselective Rhodium(III)-Catalyzed Markovnikov Hydroboration of Unactivated Terminal Alkenes. Journal of the American Chemical Society. PMID 28665124 DOI: 10.1021/Jacs.7B05149  0.392
2017 Aichhorn S, Bigler R, Myers EL, Aggarwal VK. Enantiospecific Synthesis of ortho-Substituted Benzylic Boronic Esters by a 1,2-Metalate Rearrangement/1,3-Borotropic Shift Sequence. Journal of the American Chemical Society. PMID 28661133 DOI: 10.1021/Jacs.7B05880  0.466
2017 Fawcett A, Pradeilles J, Wang Y, Mutsuga T, Myers EL, Aggarwal VK. Photoinduced decarboxylative borylation of carboxylic acids. Science (New York, N.Y.). PMID 28619717 DOI: 10.1126/Science.Aan3679  0.39
2017 Aggarwal VK, Collins B, Wilson C, Myers E. Asymmetric Synthesis of Secondary and Tertiary Boronic Esters. Angewandte Chemie (International Ed. in English). PMID 28525685 DOI: 10.1002/Anie.201701963  0.446
2017 Blair DJ, Tanini D, Bateman JM, Scott HK, Myers EL, Aggarwal VK. Selective uni- and bidirectional homologation of diborylmethane. Chemical Science. 8: 2898-2903. PMID 28451355 DOI: 10.1039/C6Sc05338F  0.419
2017 Collins BSL, Wilson CM, Myers EL, Aggarwal VK. Asymmetrische Synthese sekundärer und tertiärer Boronsäureester Angewandte Chemie. 129: 11860-11894. DOI: 10.1002/Ange.201701963  0.356
2016 Armstrong RJ, García-Ruiz C, Myers EL, Aggarwal VK. Stereodivergent Olefination of Enantioenriched Boronic Esters. Angewandte Chemie (International Ed. in English). PMID 27958668 DOI: 10.1002/Anie.201610387  0.411
2016 Fawcett A, Nitsch D, Ali M, Bateman JM, Myers EL, Aggarwal VK. Regio- and Stereoselective Homologation of 1,2-Bis(Boronic Esters): Stereocontrolled Synthesis of 1,3-Diols and Sch 725674. Angewandte Chemie (International Ed. in English). PMID 27781356 DOI: 10.1002/Anie.201608406  0.455
2016 Blair DJ, Zhong S, Hesse MJ, Zabaleta N, Myers EL, Aggarwal VK. Full chirality transfer in the synthesis of hindered tertiary boronic esters under in situ lithiation-borylation conditions. Chemical Communications (Cambridge, England). PMID 27002235 DOI: 10.1039/C6Cc00536E  0.389
2016 Wang Y, Noble A, Myers EL, Aggarwal VK. Enantiospecific Alkynylation of Alkylboronic Esters. Angewandte Chemie (International Ed. in English). PMID 26934427 DOI: 10.1002/Anie.201600599  0.423
2016 Casoni G, Myers EL, Aggarwal VK. Synthesis of 3-Aryl-1-aminopropane Derivatives: Lithiation-Borylation-Ring-Opening of Azetidinium Ions Synthesis (Germany). 48: 3241-3253. DOI: 10.1055/S-0035-1562447  0.403
2014 Myers E, Herrero-Gómez E, Albrecht I, Lachs J, Mayer P, Hanni M, Ochsenfeld C, Trauner D. Total synthesis of the proposed structure of trichodermatide A. The Journal of Organic Chemistry. 79: 9812-7. PMID 25166497 DOI: 10.1021/Jo501206K  0.348
2009 Myers EL, Raines RT. A phosphine-mediated conversion of azides into diazo compounds. Angewandte Chemie (International Ed. in English). 48: 2359-63. PMID 19035612 DOI: 10.1002/Anie.200804689  0.536
2009 Myers EL, Raines RT. ChemInform Abstract: A Phosphine-Mediated Conversion of Azides into Diazo Compounds. Cheminform. 40. DOI: 10.1002/chin.200927046  0.454
2009 Myers E, Raines R. Inside Cover: A Phosphine-Mediated Conversion of Azides into Diazo Compounds (Angew. Chem. Int. Ed. 13/2009) Angewandte Chemie International Edition. 48: 2246-2246. DOI: 10.1002/Anie.200990061  0.504
2009 Myers E, Raines R. Innentitelbild: A Phosphine-Mediated Conversion of Azides into Diazo Compounds (Angew. Chem. 13/2009) Angewandte Chemie. 121: 2280-2280. DOI: 10.1002/Ange.200990063  0.466
2007 Palmelund A, Myers EL, Tai LR, Tisserand S, Butts CP, Aggarwal VK. A new manifold for the Morita reaction: diene synthesis from simple aldehydes and acrylates/acrylonitrile mediated by phosphines. Chemical Communications (Cambridge, England). 4128-30. PMID 17925951 DOI: 10.1039/B709157E  0.447
2007 Myers EL, de Vries JG, Aggarwal VK. Reactions of iminium ions with Michael acceptors through a Morita-Baylis-Hillman-type reaction: enantiocontrol and applications in synthesis. Angewandte Chemie (International Ed. in English). 46: 1893-6. PMID 17278162 DOI: 10.1002/Anie.200604715  0.373
2006 Myers EL, Butts CP, Aggarwal VK. BF3.OEt2 and TMSOTf: A synergistic combination of Lewis acids. Chemical Communications (Cambridge, England). 4434-6. PMID 17057868 DOI: 10.1039/B611333H  0.301
2004 Fader LD, Myers EL, Tsantrizos YS. Synthesis of novel analogs of aromatic peptide nucleic acids (APNAs) with modified conformational and electrostatic properties Tetrahedron. 60: 2235-2246. DOI: 10.1016/J.Tet.2004.01.026  0.315
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