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Dieter Enders

Institute of Organic Chemistry

RWTH Aachen University

Landoltweg 1

52074 Aachen

Germany

[email]@rwth-aachen.de

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074 Aachen, Germany. 2000 - 2013
  • Institut für Organische Chemie der Rheinisch-Westfälischen Technischen Hochschule Aachen, Professor-Pirlet-Strasse 1, D-52074 Aachen, Germany. 2001 - 2005

References

  1. N-Heterocyclic carbene catalyzed synthesis of oxime esters. Enders, D., Grossmann, A., Van Craen, D. Org. Biomol. Chem. (2013) [Pubmed]
  2. Quadruple domino organocatalysis: an asymmetric aza-Michael/Michael/Michael/aldol reaction sequence leading to tetracyclic indole structures with six stereocenters. Enders, D., Greb, A., Deckers, K., Selig, P., Merkens, C. Chemistry (2012) [Pubmed]
  3. Organocatalytic one-pot asymmetric synthesis of 4H,5H-pyrano[2,3-c]pyrazoles. Enders, D., Grossmann, A., Gieraths, B., Düzdemir, M., Merkens, C. Org. Lett. (2012) [Pubmed]
  4. Chiral quaternary phosphonium salts: a new class of organocatalysts. Enders, D., Nguyen, T.V. Org. Biomol. Chem. (2012) [Pubmed]
  5. Synthesis and application of the first planar chiral strong brønsted acid organocatalysts. Enders, D., Ludwig, M., Raabe, G. Chirality (2012) [Pubmed]
  6. Organocatalytic asymmetric synthesis of polyfunctionalized 3-(cyclohexenylmethyl)-indoles via a quadruple domino Friedel-Crafts-type/Michael/Michael/aldol condensation reaction. Enders, D., Wang, C., Mukanova, M., Greb, A. Chem. Commun. (Camb.) (2010) [Pubmed]
  7. N-heterocyclic carbene catalysed asymmetric cross-benzoin reactions of heteroaromatic aldehydes with trifluoromethyl ketones. Enders, D., Grossmann, A., Fronert, J., Raabe, G. Chem. Commun. (Camb.) (2010) [Pubmed]
  8. Organocatalytic asymmetric aza-Michael additions. Enders, D., Wang, C., Liebich, J.X. Chemistry (2009) [Pubmed]
  9. Asymmetric synthesis of beta-nitro ketones via Michael addition of lithiated alpha-amino nitriles to nitroalkenes. Enders, D., Förster, D., Raabe, G., Bats, J.W. J. Org. Chem. (2008) [Pubmed]
  10. Asymmetric Brønsted acid catalyzed isoindoline synthesis: enhancement of enantiomeric ratio by stereoablative kinetic resolution. Enders, D., Narine, A.A., Toulgoat, F., Bisschops, T. Angew. Chem. Int. Ed. Engl. (2008) [Pubmed]
  11. Asymmetric synthesis of (+)-altholactone: a styryllactone isolated from various Goniothalamus species. Enders, D., Barbion, J. Chemistry (2008) [Pubmed]
  12. Organocatalytic asymmetric domino reactions: a cascade consisting of a Michael addition and an aldehyde alpha-alkylation. Enders, D., Wang, C., Bats, J.W. Angew. Chem. Int. Ed. Engl. (2008) [Pubmed]
  13. Asymmetric intermolecular Stetter reactions catalyzed by a novel triazolium derived N-heterocyclic carbene. Enders, D., Han, J., Henseler, A. Chem. Commun. (Camb.) (2008) [Pubmed]
  14. Lessons from nature: biomimetic organocatalytic carbon-carbon bond formations. Enders, D., Narine, A.A. J. Org. Chem. (2008) [Pubmed]
  15. Asymmetric total synthesis of (-)-pironetin employing the SAMP/RAMP hydrazone methodology. Enders, D., Dhulut, S., Steinbusch, D., Herrbach, A. Chemistry (2007) [Pubmed]
  16. Organocatalytic one-pot asymmetric synthesis of functionalized tricyclic carbon frameworks from a triple-cascade/Diels-Alder sequence. Enders, D., Hüttl, M.R., Runsink, J., Raabe, G., Wendt, B. Angew. Chem. Int. Ed. Engl. (2007) [Pubmed]
  17. Asymmetric organocatalytic domino reactions. Enders, D., Grondal, C., Hüttl, M.R. Angew. Chem. Int. Ed. Engl. (2007) [Pubmed]
  18. Proline organocatalysis as a new tool for the asymmetric synthesis of ulosonic acid precursors. Enders, D., Gasperi, T. Chem. Commun. (Camb.) (2007) [Pubmed]
  19. Asymmetric nucleophilic glyoxylation through a metalated alpha-aminonitrile derivative in Michael additions to nitroalkenes. Enders, D., Bonten, M.H., Raabe, G. Angew. Chem. Int. Ed. Engl. (2007) [Pubmed]
  20. Organocatalysis by N-heterocyclic carbenes. Enders, D., Niemeier, O., Henseler, A. Chem. Rev. (2007) [Pubmed]
  21. Asymmetric intramolecular crossed-benzoin reactions by N-heterocyclic carbene catalysis. Enders, D., Niemeier, O., Balensiefer, T. Angew. Chem. Int. Ed. Engl. (2006) [Pubmed]
  22. A direct organocatalytic entry to sphingoids: asymmetric synthesis of D-arabino- and L-ribo-phytosphingosine. Enders, D., Palecek, J., Grondal, C. Chem. Commun. (Camb.) (2006) [Pubmed]
  23. Control of four stereocentres in a triple cascade organocatalytic reaction. Enders, D., Hüttl, M.R., Grondal, C., Raabe, G. Nature (2006) [Pubmed]
  24. Direct organocatalytic de novo synthesis of carbohydrates. Enders, D., Grondal, C. Angew. Chem. Int. Ed. Engl. (2005) [Pubmed]
  25. The dihydroxyacetone unit--a versatile C(3) building block in organic synthesis. Enders, D., Voith, M., Lenzen, A. Angew. Chem. Int. Ed. Engl. (2005) [Pubmed]
  26. Asymmetric synthesis of the 1-epi aglycon of the cripowellins A and B. Enders, D., Lenzen, A., Raabe, G. Angew. Chem. Int. Ed. Engl. (2005) [Pubmed]
  27. Asymmetric synthesis of selectively protected amino sugars and derivatives by a direct organocatalytic Mannich reaction. Enders, D., Grondal, C., Vrettou, M., Raabe, G. Angew. Chem. Int. Ed. Engl. (2005) [Pubmed]
  28. Asymmetric total synthesis of the 1-epi-aglycon of the cripowellins A and B. Enders, D., Lenzen, A., Backes, M., Janeck, C., Catlin, K., Lannou, M.I., Runsink, J., Raabe, G. J. Org. Chem. (2005) [Pubmed]
  29. Nucleophilic carbenes in asymmetric organocatalysis. Enders, D., Balensiefer, T. Acc. Chem. Res. (2004) [Pubmed]
  30. First asymmetric synthesis of (-)-lintetralin via intramolecular Friedel-Crafts-type cyclization. Enders, D., Del Signore, G., Berner, O.M. Chirality (2003) [Pubmed]
  31. Asymmetric total synthesis of (-)-callystatin A and (-)-20-epi-callystatin A employing chemical and biological methods. Enders, D., Vicario, J.L., Job, A., Wolberg, M., Müller, M. Chemistry (2002) [Pubmed]
  32. The first highly efficient asymmetric synthesis of alpha-substituted methyl sulfonates. Enders, D., Vignola, N., Berner, O.M., Bats, J.W. Angew. Chem. Int. Ed. Engl. (2002) [Pubmed]
  33. An efficient nucleophilic carbene catalyst for the asymmetric benzoin condensation. Enders, D., Kallfass, U. Angew. Chem. Int. Ed. Engl. (2002) [Pubmed]
  34. Asymmetric synthesis of alpha-branched primary amines on solid support via novel hydrazine resins. Enders, D., Kirchhoff, J.H., Köbberling, J., Peiffer, T.H. Org. Lett. (2001) [Pubmed]
  35. Efficient asymmetric synthesis of alpha-trifluoromethyl-substituted primary amines via nucleophilic 1,2-addition to trifluoroacetaldehyde SAMP- or RAMP-hydrazone. Enders, D., Funabiki, K. Org. Lett. (2001) [Pubmed]
  36. Diastereo- and enantioselective synthesis of alpha,beta-disubstituted gamma-nitro methyl sulfonates. Enders, D., Berner, O.M., Vignola, N., Bats, J.W. Chem. Commun. (Camb.) (2001) [Pubmed]
  37. Efficient asymmetric synthesis of alpha-alkylated 1, 4-cyclohexanedione derivatives, important chiral building blocks in the synthesis of natural products. Enders, D., Nühring, A., Runsink, J. Chirality (2000) [Pubmed]
  38. Diastereo- and enantioselective total synthesis of stigmatellin A. Enders, D., Geibel, G., Osborne, S. Chemistry (2000) [Pubmed]
 
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