Heather E. Burks, Ph.D.
Affiliations: | Chemistry | Novartis, Basel, Basel-Stadt, France |
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"Heather Burks"Mean distance: 8.36
Parents
Sign in to add mentor| Jeffrey N. Johnston | research assistant | 2002-2003 | Indiana | |
| James P. Morken | grad student | 2003-2008 | Boston College | |
| (Transition-metal-catalyzed enantioselective synthesis and functionalization of 1,2- and 1,4-bis(boronate)esters.) | ||||
| F. Dean Toste | post-doc | 2008-2009 | ||
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Publications
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| Rauniyar V, Wang ZJ, Burks HE, et al. (2022) Correction to "Enantioselective Synthesis of Highly Substituted Furans by a Copper(II)-Catalyzed Cycloisomerization-Indole Addition Reaction". Journal of the American Chemical Society. 144: 13981 |
| Rauniyar V, Wang ZJ, Burks HE, et al. (2011) Enantioselective synthesis of highly substituted furans by a copper(II)-catalyzed cycloisomerization-indole addition reaction. Journal of the American Chemical Society. 133: 8486-9 |
| Rauniyar V, Wang ZJ, Burks HE, et al. (2011) Synthesis of Chiral Furans by a Copper-Catalyzed Domino Process Synfacts. 2011: 863-863 |
| Burks HE, Kliman LT, Morken JP. (2009) Asymmetric 1,4-dihydroxylation of 1,3-dienes by catalytic enantioselective diboration. Journal of the American Chemical Society. 131: 9134-5 |
| Burks HE, Kliman LT, Morken JP. (2009) Platinum-Catalyzed Asymmetric 1,4-Dihydroxylationof 1,3-Dienes Synfacts. 2009: 988-988 |
| Burks HE, Morken JP. (2007) Catalytic enantioselective diboration, disilation and silaboration: new opportunities for asymmetric synthesis. Chemical Communications (Cambridge, England). 4717-25 |
| Burks HE, Liu S, Morken JP. (2007) Development, mechanism, and scope of the palladium-catalyzed enantioselective allene diboration. Journal of the American Chemical Society. 129: 8766-73 |
| Woodward AR, Burks HE, Chan LM, et al. (2006) Catalytic Asymmetric Allene Diboration/Allylation/Functionalization Synfacts. 2006: 154-154 |
| Woodward AR, Burks HE, Chan LM, et al. (2005) Concatenated catalytic asymmetric allene diboration/allylation/functionalization. Organic Letters. 7: 5505-7 |
| Srinivasan JM, Burks HE, Smith CR, et al. (2005) Free radical-mediated aryl amination: A practical synthesis of (R)- and (S)-7-azaindoline α-amino acid Synthesis. 330-333 |