Tyler Winslow Wilson - Publications

Affiliations: 
2006-2011 Chemistry University of Illinois, Urbana-Champaign, Urbana-Champaign, IL 

15 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
2015 Lee T, Wilson TW, Berg R, Ryberg P, Hartwig JF. Rhodium-catalyzed enantioselective silylation of arene C-h bonds: desymmetrization of diarylmethanols. Journal of the American Chemical Society. 137: 6742-5. PMID 25948056 DOI: 10.1021/Jacs.5B03091  0.357
2015 Denmark SE, Wilson TW, Burk MT. ChemInform Abstract: Enantioselective Construction of Quaternary Stereogenic Carbon Atoms by the Lewis Base Catalyzed Additions of Silyl Ketene Imines to Aldehydes. Cheminform. 46: no-no. DOI: 10.1002/chin.201506105  0.525
2014 Denmark SE, Wilson TW, Burk MT. Enantioselective construction of quaternary stereogenic carbon atoms by the Lewis base catalyzed additions of silyl ketene imines to aldehydes. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 9268-79. PMID 25043283 DOI: 10.1002/Chem.201403342  0.692
2014 West R, Samedov K, Percival PW, Jutzi P, Denmark SE, Wilson TW, Burk MT, Pinkert D, Limberg C, Büchner C, Lichtenstein L, Yu X, Boscoboinik JA, Yang B, Kaden WE, et al. Cover Picture: Silicon Meets Cyclotron: Muon Spin Resonance of Organosilicon Radicals / The Pentamethylcyclopentadienylsilicon(II) Cation: Synthesis, Characterization, and Reactivity / Enantioselective Construction of Quaternary Stereogenic Carbon Atoms b Chemistry - a European Journal. 20: 9141-9141. DOI: 10.1002/Chem.201490122  0.474
2013 Denmark SE, Wilson TW. ChemInform Abstract: Silyl Ketene Imines: Highly Versatile Nucleophiles for Catalytic, Asymmetric Synthesis Cheminform. 44: no-no. DOI: 10.1002/chin.201310219  0.604
2012 Denmark SE, Wilson TW. Silyl ketene imines: highly versatile nucleophiles for catalytic, asymmetric synthesis. Angewandte Chemie (International Ed. in English). 51: 9980-92. PMID 22968901 DOI: 10.1002/Anie.201202139  0.651
2012 Denmark SE, Wilson TW. Lewis base catalyzed enantioselective additions of an N-silyl vinylketene imine. Angewandte Chemie (International Ed. in English). 51: 3236-9. PMID 22351382 DOI: 10.1002/Anie.201108795  0.63
2012 Denmark SE, Wilson TW. ChemInform Abstract: Lewis Base Catalyzed Enantioselective Additions of an N-Silyl Vinylketene Imine. Cheminform. 43: no-no. DOI: 10.1002/chin.201233075  0.509
2012 Denmark SE, Wilson TW. Silylketenimine - vielseitige Nucleophile für die katalytische asymmetrische Synthese Angewandte Chemie. 124: 10120-10132. DOI: 10.1002/Ange.201202139  0.473
2011 Denmark S, Wilson T. Lewis Base Catalyzed Asymmetric Aldol Addition of Oxyketene Imines to Aldehydes Synfacts. 2011: 0177-0177. DOI: 10.1055/s-0030-1259261  0.621
2010 Denmark SE, Wilson TW. N-silyl oxyketene imines are underused yet highly versatile reagents for catalytic asymmetric synthesis. Nature Chemistry. 2: 937-43. PMID 20966949 DOI: 10.1038/Nchem.857  0.642
2010 Denmark SE, Wilson TW. Construction of quaternary stereogenic carbon centers by the Lewis base catalyzed conjugate addition of silyl ketene imines to α,β- unsaturated aldehydes and ketones Synlett. 1723-1728. DOI: 10.1055/S-0029-1219963  0.607
2010 Denmark SE, Wilson TW. ChemInform Abstract: Construction of Quaternary Stereogenic Carbon Centers by the Lewis Base Catalyzed Conjugate Addition of Silyl Ketene Imines to α,β-Unsaturated Aldehydes and Ketones. Cheminform. 41: no-no. DOI: 10.1002/chin.201046068  0.5
2007 Denmark SE, Wilson TW, Burk MT, Heemstra JR. Enantioselective construction of quaternary stereogenic carbons by the Lewis base catalyzed additions of silyl ketene imines to aldehydes. Journal of the American Chemical Society. 129: 14864-5. PMID 17988135 DOI: 10.1021/Ja077134Y  0.671
2007 Denmark SE, Barsanti PA, Beutner GL, Wilson TW. Enantioselective ring opening of epoxides with silicon tetrachloride in the presence of a chiral lewis base: Mechanism studies Advanced Synthesis and Catalysis. 349: 566-582. DOI: 10.1002/Adsc.200600551  0.662
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