Year |
Citation |
Score |
2018 |
Haley HMS, Hill AG, Greenwood AI, Woerly EM, Rienstra CM, Burke MD. Peridinin Is an Exceptionally Potent and Membrane-Embedded Inhibitor of Bilayer Lipid Peroxidation. Journal of the American Chemical Society. PMID 30388000 DOI: 10.1021/Jacs.8B06933 |
0.53 |
|
2016 |
Woerly E, Banik SM, Jacobsen EN. Enantioselective, Catalytic Fluorolactonization Reactions with a Nucleophilic Fluoride Source. Journal of the American Chemical Society. PMID 27709922 DOI: 10.1021/Jacs.6B09499 |
0.691 |
|
2014 |
Woerly EM, Roy J, Burke MD. Synthesis of most polyene natural product motifs using just 12 building blocks and one coupling reaction Nature Chemistry. 6: 484-491. PMID 24848233 DOI: 10.1038/Nchem.1947 |
0.704 |
|
2014 |
Woerly EM, Roy J, Burke MD. Erratum: Synthesis of most polyene natural product motifs using just 12 building blocks and one coupling reaction [Nature Chemistry 6, 484-491 (2014), 10.1038/nchem.1975] Nature Chemistry. 6. DOI: 10.1038/Nchem.1975 |
0.693 |
|
2013 |
Woerly EM, Miller JE, Burke MD. (1-bromovinyl)-MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis. Tetrahedron. 69. PMID 24347693 DOI: 10.1016/J.Tet.2013.05.050 |
0.714 |
|
2012 |
Dick GR, Woerly EM, Burke MD. A general solution for the 2-pyridyl problem Angewandte Chemie - International Edition. 51: 2667-2672. PMID 22287537 DOI: 10.1002/Anie.201108608 |
0.566 |
|
2011 |
Woerly EM, Struble JR, Palyam N, O'Hara SP, Burke MD. (Z)-(2-bromovinyl)-MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis. Tetrahedron. 67: 4333-4343. PMID 22753994 DOI: 10.1016/J.Tet.2011.04.021 |
0.689 |
|
2011 |
Woerly EM, Struble JR, Palyam N, O'Hara SP, Burke MD. (Z)-(2-bromovinyl)-MIDA boronate: A readily accessible and highly versatile building block for small molecule synthesis Tetrahedron. 67: 4333-4343. DOI: 10.1016/j.tet.2011.04.021 |
0.687 |
|
2010 |
Woerly EM, Cherney AH, Davis EK, Burke MD. Stereoretentive suzuki-miyaura coupling of haloallenes enables fully stereocontrolled access to (-)-Peridinin Journal of the American Chemical Society. 132: 6941-6943. PMID 20441218 DOI: 10.1021/Ja102721P |
0.729 |
|
2010 |
Woerly EM, Cherney AH, Davis EK, Burke MD. Stereoretentive Suzuki-Miyaura Coupling of Haloallenes Synfacts. 2010: 933-933. DOI: 10.1055/S-0030-1257753 |
0.572 |
|
2010 |
Woerly EM, Cherney AH, Davis EK, Burke MD. ChemInform Abstract: Stereoretentive Suzuki-Miyaura Coupling of Haloallenes Enables Fully Stereocontrolled Access to (-)-Peridinin (Ib). Cheminform. 41: no-no. DOI: 10.1002/chin.201043207 |
0.576 |
|
2009 |
Scott WL, Alsina J, Audu CO, Babaev E, Cook L, Dage JL, Goodwin LA, Martynow JG, Matosiuk D, Royo M, Smith JG, Strong AT, Wickizer K, Woerly EM, Zhou Z, et al. Distributed Drug Discovery, Part 2: global rehearsal of alkylating agents for the synthesis of resin-bound unnatural amino acids and virtual D(3) catalog construction. Journal of Combinatorial Chemistry. 11: 14-33. PMID 19105725 DOI: 10.1021/Cc800184V |
0.415 |
|
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