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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