Chris Galliford
Affiliations: | 2002-2007 | Northwestern University, Evanston, IL |
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"Chris Galliford"Mean distance: 8.3 | S | N | B | C | P |
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Sign in to add mentor| Karl A. Scheidt | grad student | 2002-2007 | Northwestern | |
| (A multi-component catalytic assembly reaction for the synthesis of nitrogen -containing heterocycles and Umpolung transformations of aldehydes and acylsilanes.) | ||||
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| Johnson PL, Renga JM, Galliford CV, et al. (2015) Synthesis of Novel Fluoropicolinate Herbicides by Cascade Cyclization of Fluoroalkyl Alkynylimines. Organic Letters. 17: 2905-7 |
| Lettan RB, Galliford CV, Woodward CC, et al. (2009) Amide enolate additions to acylsilanes: in situ generation of unusual and stereoselective homoenolate equivalents. Journal of the American Chemical Society. 131: 8805-14 |
| Galliford CV, Scheidt KA. (2008) An unusual dianion equivalent from acylsilanes for the synthesis of substituted beta-keto esters. Chemical Communications (Cambridge, England). 1926-8 |
| Galliford CV, Scheidt KA. (2007) Pyrrolidinyl-spirooxindole natural products as inspirations for the development of potential therapeutic agents. Angewandte Chemie (International Ed. in English). 46: 8748-58 |
| Galliford CV, Martenson JS, Stern C, et al. (2007) A highly diastereoselective, catalytic three-component assembly reaction for the synthesis of spiropyrrolidinyloxindoles. Chemical Communications (Cambridge, England). 631-3 |
| Galliford CV, Scheidt KA. (2007) Catalytic multicomponent reactions for the synthesis of N-aryl trisubstituted pyrroles. The Journal of Organic Chemistry. 72: 1811-3 |
| Scheidt K, Galliford C. (2007) Rh-Catalyzed Synthesis of N-Aryl Trisubstituted Pyrroles Synfacts. 2007: 0474-0474 |
| Scheidt K, Galliford C, Martenson J, et al. (2007) Spirooxindoles from a 3-CR of Imines, Diazoesters, and Olefin Dipolarophiles Synfacts. 2007: 0361-0361 |
| Scheidt K, II R, Reynolds T, et al. (2007) Synthesis of Tertiary β-Hydroxy Amides via Acylsilanes Synfacts. 2007: 0303-0303 |
| Galliford C, Scheidt K. (2007) Natürliche Pyrrolidinylspirooxindole als Vorlagen für die Entwicklung medizinischer Wirkstoffe Angewandte Chemie. 119: 8902-8912 |