Jakub Svenda, Ph.D.
Affiliations: | 2010 | Harvard University, Cambridge, MA, United States |
Area:
synthesis of natural productsGoogle:
"Jakub Svenda"Mean distance: 8.28 | S | N | B | C | P |
Parents
Sign in to add mentor| Andrew G. Myers | grad student | 2010 | Harvard | |
| (A convergent synthetic route to trioxacarcins.) | ||||
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| 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 |