Jakub Svenda, Ph.D.

2010 Harvard University, Cambridge, MA, United States 
synthesis of natural products
"Jakub Svenda"
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Andrew G. Myers grad student 2010 Harvard
 (A convergent synthetic route to trioxacarcins.)
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Szczepanik PM, Mikhaylov AA, Hylse O, et al. (2022) Convergent Assembly of the Tricyclic Labdane Core Enables Synthesis of Diverse Forskolin-like Molecules. Angewandte Chemie (International Ed. in English)
Tharra PR, Mikhaylov AA, Švejkar J, et al. (2022) Short Synthesis of (+)-Actinobolin: Simple Entry to Complex Small-Molecule Inhibitors of Protein Synthesis. Angewandte Chemie (International Ed. in English). e202116520
Jachak GR, Tharra PR, Sevelda P, et al. (2021) Stereocontrolled Synthesis of Pseurotin A. The Journal of Organic Chemistry
Vojáčková P, Michalska L, Nečas M, et al. (2020) Stereocontrolled Synthesis of (-)-Bactobolin A. Journal of the American Chemical Society. 142: 7306-7311
Vojáčková P, Chalupa D, Prieboj J, et al. (2018) Enantioselective Conjugate Additions of 2-Alkoxycarbonyl-3(2 H)-furanones. Organic Letters
Hylse O, Maier L, Kučera R, et al. (2017) A concise synthesis of forskolin. Angewandte Chemie (International Ed. in English)
Chalupa D, Vojáčková P, Partl J, et al. (2017) Enantioselective Synthesis of Cephalimysins B and C. Organic Letters
Hill N, Paruch K, Švenda J. (2016) Late-stage annulative convergency in natural product synthesis Tetrahedron. 72: 3345-3368
Kučera R, Hylse O, Babiak M, et al. (2015) Facile rearrangements of a vinylogous α-hydroxy-β-dicarbonyl substrate involving an apparent oxirane C–C bond scission Tetrahedron Letters. 56: 6171-6173
Smaltz DJ, Švenda J, Myers AG. (2012) Diastereoselective additions of allylmetal reagents to free and protected syn-α,β-dihydroxyketones enable efficient synthetic routes to methyl trioxacarcinoside A. Organic Letters. 14: 1812-5
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