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Jakub Svenda, Ph.D. - Publications

Affiliations: 
2010 Harvard University, Cambridge, MA, United States 
Area:
synthesis of natural products
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13 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Szczepanik PM, Mikhaylov AA, Hylse O, Kučera R, Daďová P, Nečas M, Kubala L, Paruch K, Švenda J. Convergent Assembly of the Tricyclic Labdane Core Enables Synthesis of Diverse Forskolin-like Molecules. Angewandte Chemie (International Ed. in English). PMID 36321750 DOI: 10.1002/anie.202213183  0.363
2022 Tharra PR, Mikhaylov AA, Švejkar J, Gysin M, Hobbie SN, Švenda J. Short Synthesis of (+)-Actinobolin: Simple Entry to Complex Small-Molecule Inhibitors of Protein Synthesis. Angewandte Chemie (International Ed. in English). e202116520. PMID 35167723 DOI: 10.1002/anie.202116520  0.386
2021 Jachak GR, Tharra PR, Sevelda P, Švenda J. Stereocontrolled Synthesis of Pseurotin A. The Journal of Organic Chemistry. PMID 34378926 DOI: 10.1021/acs.joc.1c01152  0.344
2020 Vojáčková P, Michalska L, Nečas M, Shcherbakov D, Böttger EC, Šponer J, Šponer JE, Švenda J. Stereocontrolled Synthesis of (-)-Bactobolin A. Journal of the American Chemical Society. 142: 7306-7311. PMID 32285674 DOI: 10.1021/Jacs.0C01554  0.502
2018 Vojáčková P, Chalupa D, Prieboj J, Nečas M, Švenda J. Enantioselective Conjugate Additions of 2-Alkoxycarbonyl-3(2 H)-furanones. Organic Letters. PMID 30375225 DOI: 10.1021/Acs.Orglett.8B03039  0.453
2017 Hylse O, Maier L, Kučera R, Perečko T, Svobodová A, Kubala L, Paruch K, Svenda J. A concise synthesis of forskolin. Angewandte Chemie (International Ed. in English). PMID 28782270 DOI: 10.1002/Anie.201706809  0.441
2017 Chalupa D, Vojáčková P, Partl J, Pavlović D, Nečas M, Švenda J. Enantioselective Synthesis of Cephalimysins B and C. Organic Letters. PMID 28157322 DOI: 10.1021/Acs.Orglett.6B03373  0.421
2016 Hill N, Paruch K, Švenda J. Late-stage annulative convergency in natural product synthesis Tetrahedron. 72: 3345-3368. DOI: 10.1016/J.Tet.2016.04.004  0.388
2015 Kučera R, Hylse O, Babiak M, Švenda J. Facile rearrangements of a vinylogous α-hydroxy-β-dicarbonyl substrate involving an apparent oxirane C–C bond scission Tetrahedron Letters. 56: 6171-6173. DOI: 10.1016/J.Tetlet.2015.09.015  0.388
2012 Smaltz DJ, Švenda J, Myers AG. 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. PMID 22404560 DOI: 10.1021/Ol300377A  0.413
2011 Švenda J, Hill N, Myers AG. A multiply convergent platform for the synthesis of trioxacarcins. Proceedings of the National Academy of Sciences of the United States of America. 108: 6709-14. PMID 21245350 DOI: 10.1073/Pnas.1015257108  0.561
2009 Svenda J, Myers AG. Anti-selective epoxidation of methyl alpha-methylene-beta-tert-butyldimethylsilyloxycarboxylate esters. Evidence for stereospecific oxygen atom transfer in a nucleophilic epoxidation process. Organic Letters. 11: 2437-40. PMID 19397300 DOI: 10.1021/Ol900665A  0.534
2004 Bower JF, Svenda J, Williams AJ, Charmant JP, Lawrence RM, Szeto P, Gallagher T. Cyclic sulfamidates as vehicles for the synthesis of substituted lactams. Organic Letters. 6: 4727-30. PMID 15575671 DOI: 10.1021/Ol048036+  0.461
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