Eddie L. Myers

Affiliations: 
2006-2009 University of Wisconsin, Madison, Madison, WI 
Google:
"Eddie Myers"
Mean distance: 8.25
 
SNBCP
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Aiken SG, Bateman JM, Liao HH, et al. (2022) Iterative synthesis of 1,3-polyboronic esters with high stereocontrol and application to the synthesis of bahamaolide A. Nature Chemistry
Myers EL, Palte MJ, Raines RT. (2019) Catalysis of Hydrogen-Deuterium Exchange Reactions by 4-Substituted Proline Derivatives. The Journal of Organic Chemistry
Mykura RC, Veth S, Varela A, et al. (2018) 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
Armstrong RJ, Nandakumar M, Dias RMP, et al. (2018) Enantiodivergent Synthesis of Allenes by Point to Axial Chirality Transfer. Angewandte Chemie (International Ed. in English)
Noble A, Mega RS, Pflästerer D, et al. (2018) Visible-Light-Mediated Decarboxylative Radical Additions to Vinyl Boronic Esters: Rapid Access to γ-Amino Boronic Esters. Angewandte Chemie (International Ed. in English)
Lorenzo P, Butts CP, Myers EL, et al. (2017) The Story behind "Synergy of Synthesis, Computation, and NMR Reveals Correct Baulamycin Structures". Biochemistry
Bootwicha T, Feilner JM, Myers EL, et al. (2017) Iterative assembly line synthesis of polypropionates with full stereocontrol. Nature Chemistry. 9: 896-902
Casoni G, Kucukdisli M, Fordham JM, et al. (2017) α-Sulfinyl Benzoates as Precursors to Li and Mg Carbenoids for the Stereoselective Iterative Homologation of Boronic Esters. Journal of the American Chemical Society
Wu J, Lorenzo P, Zhong S, et al. (2017) Synergy of synthesis, computation and NMR reveals correct baulamycin structures. Nature. 547: 436-440
Smith JR, Collins BSL, Hesse MJ, et al. (2017) Enantioselective Rhodium(III)-Catalyzed Markovnikov Hydroboration of Unactivated Terminal Alkenes. Journal of the American Chemical Society
See more...