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Chemical Communications (Cambridge, England)|November 16, 2007
Catalytic enantioselective diboration, disilation and silaboration: new opportunities for asymmetric synthesisHeather E Burks, James P MorkenJournal of the American Chemical Society|June 26, 2007
Development, mechanism, and scope of the palladium-catalyzed enantioselective allene diborationHeather E Burks, Shubin Liu, James P MorkenJournal of the American Chemical Society|June 10, 2009
Asymmetric 1,4-dihydroxylation of 1,3-dienes by catalytic enantioselective diborationHeather E Burks, Laura T Kliman, James P MorkenJournal of the American Chemical Society|May 13, 2011
Enantioselective synthesis of highly substituted furans by a copper(II)-catalyzed cycloisomerization-indole addition reactionVivek Rauniyar, Z Jane Wang, Heather E Burks, et al.Organic Letters|November 18, 2005
Concatenated catalytic asymmetric allene diboration/allylation/functionalizationAngela R Woodward, Heather E Burks, Louis M Chan, et al.Synthesis|October 24, 2022
Free Radical-Mediated Aryl Amination: A Practical Synthesis of (R)- and (S)-7-Azaindoline α-Amino AcidJayasree M Srinivasan, Heather E Burks, Colin R Smith, et al.Journal of the American Chemical Society|December 17, 2004
Palladium-catalyzed enantioselective diboration of prochiral allenesNicholas F Pelz, Angela R Woodward, Heather E Burks, et al.Journal of Medicinal Chemistry|March 16, 2017
Discovery of an Acrylic Acid Based Tetrahydroisoquinoline as an Orally Bioavailable Selective Estrogen Receptor Degrader for ERα+ Breast CancerHeather E Burks, Tinya Abrams, Christina A Kirby, et al.Journal of Medicinal Chemistry|March 23, 2018
Discovery of LSZ102, a Potent, Orally Bioavailable Selective Estrogen Receptor Degrader (SERD) for the Treatment of Estrogen Receptor Positive Breast CancerGeorge S Tria, Tinya Abrams, Jason Baird, et al.Pageof 1