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Katrina L Jackson

Showing results (1-10 of 12) with videos related to

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Chemical Reviews|June 19, 2009
The halichondrins and E7389Katrina L Jackson, James A Henderson, Andrew J Phillips
Organic Letters|November 15, 2007
Highly functionalized pyranopyrans from furans: a synthesis of the C27-C38 and C44-C53 subunits of norhalichondrin BJames A Henderson, Katrina L Jackson, Andrew J Phillips
Tetrahedron|March 16, 2010
Scalable and efficient synthesis of the mycolactone coreKatrina L Jackson, Wenju Li, Chi-Li Chen, et al.
Angewandte Chemie (International Ed. in English)|February 13, 2009
A total synthesis of norhalichondrin BKatrina L Jackson, James A Henderson, Hajime Motoyoshi, et al.
Tetrahedron Letters|June 16, 2010
A synthesis of the C1-C15 domain of the halichondrinsKatrina L Jackson, James A Henderson, Jonathan C Morris, et al.
Organic Letters|August 29, 2012
Synthesis and structure of two new mycolactones isolated from M. ulcerans subsp. shinshuenseSudhir M Hande, Yuko Kazumi, W George Lai, et al.
Chemical Communications (Cambridge, England)|December 22, 2009
Heterogeneity in the stereochemistry of mycolactones isolated from M. marinum: toxins produced by fresh vs. saltwater fish pathogensHan-Je Kim, Katrina L Jackson, Yoshito Kishi, et al.
Journal of Medicinal Chemistry|November 24, 2025
Discovery of CFT8634, a Potent, Selective, and Orally Bioavailable Heterobifunctional Degrader of BRD9Katrina L Jackson, Ning Yin, Roman V Agafonov, et al.
Cancer Research|October 28, 2025
CFT1946 is an Orally Available Brain-Penetrant BRAFV600-Mutant Degrader that Overcomes BRAF Inhibitor ResistanceBridget T Kreger, Yanke Liang, Nicole M Reilly, et al.
Journal of Medicinal Chemistry|December 6, 2021
Discovery of Novel, Orally Bioavailable Pyrimidine Ether-Based Inhibitors of ELOVL1Michael J Boyd, Philip N Collier, Michael P Clark, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Chemical Reviews|June 19, 2009
The halichondrins and E7389Katrina L Jackson, James A Henderson, Andrew J Phillips
Organic Letters|November 15, 2007
Highly functionalized pyranopyrans from furans: a synthesis of the C27-C38 and C44-C53 subunits of norhalichondrin BJames A Henderson, Katrina L Jackson, Andrew J Phillips
Tetrahedron|March 16, 2010
Scalable and efficient synthesis of the mycolactone coreKatrina L Jackson, Wenju Li, Chi-Li Chen, et al.
Angewandte Chemie (International Ed. in English)|February 13, 2009
A total synthesis of norhalichondrin BKatrina L Jackson, James A Henderson, Hajime Motoyoshi, et al.
Tetrahedron Letters|June 16, 2010
A synthesis of the C1-C15 domain of the halichondrinsKatrina L Jackson, James A Henderson, Jonathan C Morris, et al.
Organic Letters|August 29, 2012
Synthesis and structure of two new mycolactones isolated from M. ulcerans subsp. shinshuenseSudhir M Hande, Yuko Kazumi, W George Lai, et al.
Chemical Communications (Cambridge, England)|December 22, 2009
Heterogeneity in the stereochemistry of mycolactones isolated from M. marinum: toxins produced by fresh vs. saltwater fish pathogensHan-Je Kim, Katrina L Jackson, Yoshito Kishi, et al.
Journal of Medicinal Chemistry|November 24, 2025
Discovery of CFT8634, a Potent, Selective, and Orally Bioavailable Heterobifunctional Degrader of BRD9Katrina L Jackson, Ning Yin, Roman V Agafonov, et al.
Cancer Research|October 28, 2025
CFT1946 is an Orally Available Brain-Penetrant BRAFV600-Mutant Degrader that Overcomes BRAF Inhibitor ResistanceBridget T Kreger, Yanke Liang, Nicole M Reilly, et al.
Journal of Medicinal Chemistry|December 6, 2021
Discovery of Novel, Orally Bioavailable Pyrimidine Ether-Based Inhibitors of ELOVL1Michael J Boyd, Philip N Collier, Michael P Clark, et al.
Pageof 2