As an emeritus professor of Synthetic Organic Chemistry Henk Hiemstra continues to contribute to the UvA chemistry research at the Van 't Hoff Institute of Molecular Sciences.
On 25 May 2018 he held his farewell lecture:
 Horst, B., Wanner, M. J., Jørgensen, S. I., Hiemstra, H., & van Maarseveen, J. H. (2018). Total Synthesis of the Ortho-Hydroxylated Protoberberines (S)-Govaniadine, (S)-Caseamine, and (S)-Clarkeanidine via a Solvent-Directed Pictet-Spengler Reaction. Journal of Organic Chemistry, 83(24), 15110-15117. https://doi.org/10.1021/acs.joc.8b02378 [details]
Horst, B., Wanner, M. J., Jørgensen, S. I., Hiemstra, H., & van Maarseveen, J. H. (2018). Total Synthesis of the Ortho-Hydroxylated Protoberberines (S)-Govaniadine, (S)-Caseamine, and (S)-Clarkeanidine via a Solvent-Directed Pictet-Spengler Reaction. Journal of Organic Chemistry, 83(24), 15110-15117. https://doi.org/10.1021/acs.joc.8b02378 [details] Steemers, L., Wanner, M. J., van Leeuwen, B. R. C., Hiemstra, H., & van Maarseveen, J. H. (2018). Attempted [2]Catenane Synthesis via a Quasi[1]catenane by a Templated Backfolding Strategy. European Journal of Organic Chemistry, 2018(7), 874-878. https://doi.org/10.1002/ejoc.201701325 [details]
Steemers, L., Wanner, M. J., van Leeuwen, B. R. C., Hiemstra, H., & van Maarseveen, J. H. (2018). Attempted [2]Catenane Synthesis via a Quasi[1]catenane by a Templated Backfolding Strategy. European Journal of Organic Chemistry, 2018(7), 874-878. https://doi.org/10.1002/ejoc.201701325 [details] Steemers, L., Wanner, M. J., Ehlers, A. W., Hiemstra, H., & van Maarseveen, J. H. (2017). A Short Covalent Synthesis of an All-Carbon-Ring [2]Rotaxane. Organic Letters, 19(9), 2342-2345. https://doi.org/10.1021/acs.orglett.7b00877 [details]
Steemers, L., Wanner, M. J., Ehlers, A. W., Hiemstra, H., & van Maarseveen, J. H. (2017). A Short Covalent Synthesis of an All-Carbon-Ring [2]Rotaxane. Organic Letters, 19(9), 2342-2345. https://doi.org/10.1021/acs.orglett.7b00877 [details] Steemers, L., Wanner, M. J., Lutz, M., Hiemstra, H., & van Maarseveen, J. H. (2017). Synthesis of spiro quasi[1]catenanes and quasi[1]rotaxanes via a templated backfolding strategy. Nature Communications, 8, Article 15392. https://doi.org/10.1038/ncomms15392 [details]
Steemers, L., Wanner, M. J., Lutz, M., Hiemstra, H., & van Maarseveen, J. H. (2017). Synthesis of spiro quasi[1]catenanes and quasi[1]rotaxanes via a templated backfolding strategy. Nature Communications, 8, Article 15392. https://doi.org/10.1038/ncomms15392 [details] Kayhan, J., Wanner, M. J., Ingemann, S., van Maarseveen, J. H., & Hiemstra, H. (2016). Consecutive Pictet-Spengler Condensations toward Bioactive 8-Benzylprotoberberines: Highly Selective Total Syntheses of (+)-Javaberine A, (+)-Javaberine B, and (-)-Latifolian A. European Journal of Organic Chemistry, 2016(22), 3705-3708. https://doi.org/10.1002/ejoc.201600764 [details]
Kayhan, J., Wanner, M. J., Ingemann, S., van Maarseveen, J. H., & Hiemstra, H. (2016). Consecutive Pictet-Spengler Condensations toward Bioactive 8-Benzylprotoberberines: Highly Selective Total Syntheses of (+)-Javaberine A, (+)-Javaberine B, and (-)-Latifolian A. European Journal of Organic Chemistry, 2016(22), 3705-3708. https://doi.org/10.1002/ejoc.201600764 [details] Kleinnijenhuis, R. A., Timmer, B. J. J., Lutteke, G., Smits, J. M. M., de Gelder, R., van Maarseveen, J. H., & Hiemstra, H. (2016). Formal synthesis of solanoeclepin A: enantioselective allene diboration and intramolecular [2+2] photocycloaddition for the construction of the tricyclic core. Chemistry - A European Journal, 22(4), 1266-1269. https://doi.org/10.1002/chem.201504894 [details]
Kleinnijenhuis, R. A., Timmer, B. J. J., Lutteke, G., Smits, J. M. M., de Gelder, R., van Maarseveen, J. H., & Hiemstra, H. (2016). Formal synthesis of solanoeclepin A: enantioselective allene diboration and intramolecular [2+2] photocycloaddition for the construction of the tricyclic core. Chemistry - A European Journal, 22(4), 1266-1269. https://doi.org/10.1002/chem.201504894 [details] Lutteke, G., Kleinnijenhuis, R. A., Beuving, R. J., de Gelder, R., Smits, J. M. M., van Maarseveen, J. H., & Hiemstra, H. (2016). Enantioselective Approach to the Right-Hand Substructure of Solanoeclepin A. European Journal of Organic Chemistry, 2016(35), 5845-5854. https://doi.org/10.1002/ejoc.201601094 [details]
Lutteke, G., Kleinnijenhuis, R. A., Beuving, R. J., de Gelder, R., Smits, J. M. M., van Maarseveen, J. H., & Hiemstra, H. (2016). Enantioselective Approach to the Right-Hand Substructure of Solanoeclepin A. European Journal of Organic Chemistry, 2016(35), 5845-5854. https://doi.org/10.1002/ejoc.201601094 [details] Pauli, G. F., Niemitz, M., Bisson, J., Lodewyk, M. W., Soldi, C., Shaw, J. T., Tantillo, D. J., Saya, J. M., Vos, K., Klein Nijenhuis, R. A., Hiemstra, H., Chen, S.-N., McAlpine, J. B., Lankin, D. C., & Friesen, J. B. (2016). Toward Structural Correctness: Aquatolide and the Importance of 1D Proton NMR FID Archiving. Journal of Organic Chemistry, 81(3), 878-889. https://doi.org/10.1021/acs.joc.5b02456 [details]
Pauli, G. F., Niemitz, M., Bisson, J., Lodewyk, M. W., Soldi, C., Shaw, J. T., Tantillo, D. J., Saya, J. M., Vos, K., Klein Nijenhuis, R. A., Hiemstra, H., Chen, S.-N., McAlpine, J. B., Lankin, D. C., & Friesen, J. B. (2016). Toward Structural Correctness: Aquatolide and the Importance of 1D Proton NMR FID Archiving. Journal of Organic Chemistry, 81(3), 878-889. https://doi.org/10.1021/acs.joc.5b02456 [details] Popovic, S., Wijsman, L., Landman, I. R., Sangster, M. F., Pastoors, D., Veldhorst, B. B., Hiemstra, H., & van Maarseveen, J. H. (2016). Fine-tuning the balance between peptide thioester cyclization and racemization. European Journal of Organic Chemistry, 2016(3), 443-446. https://doi.org/10.1002/ejoc.201501366 [details]
Popovic, S., Wijsman, L., Landman, I. R., Sangster, M. F., Pastoors, D., Veldhorst, B. B., Hiemstra, H., & van Maarseveen, J. H. (2016). Fine-tuning the balance between peptide thioester cyclization and racemization. European Journal of Organic Chemistry, 2016(3), 443-446. https://doi.org/10.1002/ejoc.201501366 [details] Breman, A. C., Telderman, S. E. M., van Santen, R. P. M., Scott, J. I., van Maarseveen, J. H., Ingemann, S., & Hiemstra, H. (2015). Cinchona alkaloid catalyzed sulfa-Michael addition reactions leading to enantiopure β-functionalized cysteines. Journal of Organic Chemistry, 80(21), 10561-10574. https://doi.org/10.1021/acs.joc.5b01660 [details]
Breman, A. C., Telderman, S. E. M., van Santen, R. P. M., Scott, J. I., van Maarseveen, J. H., Ingemann, S., & Hiemstra, H. (2015). Cinchona alkaloid catalyzed sulfa-Michael addition reactions leading to enantiopure β-functionalized cysteines. Journal of Organic Chemistry, 80(21), 10561-10574. https://doi.org/10.1021/acs.joc.5b01660 [details] Ruiz-Olalla, A., Würdemann, M. A., Wanner, M. J., Ingemann, S., van Maarseveen, J. H., & Hiemstra, H. (2015). Organocatalytic Enantioselective Pictet-Spengler Approach to Biologically Relevant 1-Benzyl-1,2,3,4-Tetrahydroisoquinoline Alkaloids. Journal of Organic Chemistry, 80(10), 5125-5132. https://doi.org/10.1021/acs.joc.5b00509 [details]
Ruiz-Olalla, A., Würdemann, M. A., Wanner, M. J., Ingemann, S., van Maarseveen, J. H., & Hiemstra, H. (2015). Organocatalytic Enantioselective Pictet-Spengler Approach to Biologically Relevant 1-Benzyl-1,2,3,4-Tetrahydroisoquinoline Alkaloids. Journal of Organic Chemistry, 80(10), 5125-5132. https://doi.org/10.1021/acs.joc.5b00509 [details] Saya, J. M., Vos, K., Klein Nijenhuis, R. A., van Maarseveen, J. H., Ingemann, S., & Hiemstra, H. (2015). Total synthesis of aquatolide. Organic Letters, 17(15), 3892-3894. https://doi.org/10.1021/acs.orglett.5b01888 [details]
Saya, J. M., Vos, K., Klein Nijenhuis, R. A., van Maarseveen, J. H., Ingemann, S., & Hiemstra, H. (2015). Total synthesis of aquatolide. Organic Letters, 17(15), 3892-3894. https://doi.org/10.1021/acs.orglett.5b01888 [details] Smeenk, L. E. J., Timmers-Parohi, D., Benschop, J. J., Puijk, W. C., Hiemstra, H., van Maarseveen, J. H., & Timmerman, P. (2015). Reconstructing the Discontinuous and Conformational β1/β 3-Loop Binding Site on hFSH/hCG by Using Highly Constrained Multicyclic Peptides. ChemBioChem, 16(1), 91-99. https://doi.org/10.1002/cbic.201402540 [details]
Smeenk, L. E. J., Timmers-Parohi, D., Benschop, J. J., Puijk, W. C., Hiemstra, H., van Maarseveen, J. H., & Timmerman, P. (2015). Reconstructing the Discontinuous and Conformational β1/β 3-Loop Binding Site on hFSH/hCG by Using Highly Constrained Multicyclic Peptides. ChemBioChem, 16(1), 91-99. https://doi.org/10.1002/cbic.201402540 [details] Wassenaar, J., Detz, R. J., de Boer, S. Y., Lutz, M., van Maarseveen, J. H., Hiemstra, H., & Reek, J. N. H. (2015). Enantioselective Synthesis of Tunable Chiral Clickphine P,N-Ligands and Their Application in Ir-Catalyzed Asymmetric Hydrogenation. Journal of Organic Chemistry, 80(7), 3634-3642. https://doi.org/10.1021/acs.joc.5b00438 [details]
Wassenaar, J., Detz, R. J., de Boer, S. Y., Lutz, M., van Maarseveen, J. H., Hiemstra, H., & Reek, J. N. H. (2015). Enantioselective Synthesis of Tunable Chiral Clickphine P,N-Ligands and Their Application in Ir-Catalyzed Asymmetric Hydrogenation. Journal of Organic Chemistry, 80(7), 3634-3642. https://doi.org/10.1021/acs.joc.5b00438 [details]