Bakary-Barry Toure, Ph.D. - Publications
Affiliations: | University of Alberta, Edmonton, Alberta, Canada |
Year | Citation | Score | |||
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2012 | Genovino J, Lagu B, Wang Y, Touré BB. Synthesis of sterically hindered enamides via a Ti-mediated condensation of amides with aldehydes and ketones. Chemical Communications (Cambridge, England). 48: 6735-7. PMID 22643736 DOI: 10.1039/c2cc32538a | 0.317 | |||
2005 | Gravel M, Toure BB, Hall DG. Practical Procedure for the Preparation of Functionalized (E)-1-Alkenylboronic Acids Including the Unprecedented 1-Alkoxycarbonyl Derivatives. Cheminform. 36. DOI: 10.1080/00304940409355974 | 0.465 | |||
2005 | Touré BB, Hall DG. Multicomponent Reactions in the Total Synthesis of Natural Products Multicomponent Reactions. 342-397. DOI: 10.1002/3527605118.ch12 | 0.445 | |||
2004 | Touré BB, Hall DG. Three-component sequential aza[4+2] cycloaddition/allylboration/retro-sulfinyl-ene reaction: a new stereocontrolled entry to palustrine alkaloids and other 2,6-disubstituted piperidines. Angewandte Chemie (International Ed. in English). 43: 2001-4. PMID 15065285 DOI: 10.1002/Anie.200353152 | 0.445 | |||
2004 | Gravel M, Touré BB, Hall DG. PRACTICAL PROCEDURE FOR THE PREPARATION OF FUNCTIONALIZED (E)-1-ALKENYLBORONIC ACIDS INCLUDING THE UNPRECEDENTED 1-ALKOXYCARBONYL DERIVATIVES Organic Preparations and Procedures International. 36: 573-579. DOI: 10.1080/00304940409355974 | 0.548 | |||
2004 | Toure BB, Hall DG. Three-Component Sequential Aza[4 + 2] Cycloaddition/Allylboration/Retro-Sulfinyl-Ene Reaction: A New Stereocontrolled Entry to Palustrine Alkaloids and Other 2,6-Disubstituted Piperidines. Cheminform. 35. DOI: 10.1002/chin.200430193 | 0.356 | |||
2003 | Touré BB, Hoveyda HR, Tailor J, Ulaczyk-Lesanko A, Hall DG. A three-component reaction for diversity-oriented synthesis of polysubstituted piperidines: solution and solid-phase optimization of the first tandem aza[4+2]/allylboration. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 466-74. PMID 12532296 DOI: 10.1002/Chem.200390049 | 0.498 | |||
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