Inhalt des Dokuments
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37.
M. König, M. Rigo, N. Chaoui, T. Tran Ngoc, J. D. Epping, J. Schmidt, P. Pachfule, J. F. Teichert, M. Drieß, A. Thomas,
Immobilization of an Iridium Pincer Complex in a Microporous Polymer for Application in Room-Temperature Gas Phase Catalysis,
Angew. Chem. Int. Ed. 2020, accepted. DOI: 10.1002/anie.202004092.
36.
L. T. Brechmann, J. F. Teichert,
Catch It if You Can: Copper-catalyzed (Transfer) Hydrogenation Reactions and Coupling Reactions by Intercepting Reactive Intermediates thereof, Synthesis 2020, 52, 2483-2496. This work has been selected as "editor's choice" and is now open access.
35.
N. O. Thiel, F. Pape, J. F. Teichert,
Homogeneous Hydrogenation with Copper Catalysts (Book Chapter) in Homogeneous Hydrogenation with Non-Precious Catalysts, Wiley, Weinheim, 2019.
34.
T. Kaicharla, B. M. Zimmermann, M. Oestreich, J. F. Teichert,
Using alcohols as simple H2-equivalents for copper-catalysed transfer semihydrogenations of alkynes,
Chem. Commun. 2019, 55, 13410-13413. This work was highlighted by ChemistryViews and by Organic Chemistry Highlights.
33.
N. O. Thiel, B. Kaewmee, T. Tran Ngoc, J. F. Teichert,
A Simple Nickel Catalyst Enabling an E-Selective Alkyne Semihydrogenation,
Chem. Eur. J. 2020, 26, 1597-1603.
32.
N. O. Thiel, L. T. Brechmann, J. F. Teichert,
Catalytic Hydrogenations with Cationic Heteroleptic Copper(I)/N-Heterocyclic Carbene Complexes,
Synlett 2019, 30, 783-786. Published as part of the Special Section 10th EuCheMS Organic Division Young Investigator Workshop.
31.
B. M. Zimmermann, S. C. K. Kobosil, J. F. Teichert,
Catalytic hydrogenation of alpha,beta-unsaturated carboxylic acid derivatives using coper(I)/N-heterocyclic carbene complexes,
Chem. Commun. 2019, 55, 2293-2296.
30.
F. Pape, L. T. Brechmann, J. F. Teichert,
Catalytic Generation and Chemoselective Transfer of Nucleophilic Hydrides from Dihydrogen,
Chem. Eur. J. 2019, 25, 985-988.
This work was featured in Organic Chemistry Highlights.
29.
M. Das, T. Kaicharla, J. F. Teichert,
Stereoselective Alkyne Hydrohalogenation by Trapping of Transfer Hydrogenation Intermediates,
Org. Lett. 2018, 20, 4926-4929. This work was highlighted in Synfacts 2018, 14, 1265 and in Organic Chemistry Highlights.
28.
J. F. Teichert,
Synthese im Blickpunkt: Benzol dearomatisieren mit Licht,
Nachr. Chem. 2017, 65, 1092-1095.
27.
T. N. T. Nguyen, N. O. Thiel, J. F. Teichert,
Copper(I)-catalysed asymmetric allylic reductions with hydrosilanes,
Chem. Commun. 2017, 53, 11686-11689.
26.
F. Pape, J. F. Teichert,
Synthese im Blickpunkt: Polyketide am Fließband,
Nachr. Chem. 2017, 65, 879 - 883.
25.
N. O. Thiel, J. F. Teichert,
Synthese im Blickpunkt: Interhalogenierung: Das Problemkind der Alkenbromierung,
Nachr. Chem. 2017, 65, 772 - 775.
24.
N. O. Thiel, S. Kemper, J. F. Teichert,
Copper(I)-catalyzed stereoselective hydrogenation of 1,3-diynes and enynes,
Tetrahedron 2017, 73, 5023-5028.
(Invited manuscript for the Symposium-in-Print on the occasion of the Tetrahedron Prize 2017 for Ben Feringa)
23.
J. F. Teichert,
Synthese im Blickpunkt: Benachbarte Stereozentren unter voller Kontrolle,
Nachr. Chem. 2017, 65, 530 - 534.
22.
M. Trunk, J. F. Teichert, A. Thomas,
Room-Temperature Activation of Hydrogen by Semi-Immobilized
Frustrated Lewis Pairs in Microporous Polymer Networks,
J. Am. Chem. Soc. 2017, 139, 3615-3618.
21.
F. Pape, J. F. Teichert,
Dealing at Arm’s Length - Catalysis with N-Heterocyclic Carbene Ligands
bearing Anionic Tethers (Microreview),
Eur. J. Org. Chem. 2017, 29, 4206-4229.
20.
F. Pape, J. F. Teichert,
Tethered NHC Ligands for Stereoselective Alkyne Semihydrogenations,
Synthesis 2017, 49, 2470-2482.
19.
J. F. Teichert,
Synthese im Blickpunkt: C-C Bindungen knüpfen mit Aktivestern,
Nachr. Chem. 2017, 65, 26-29.
18.
E. Korytiaková, N. O. Thiel, F. Pape and J. F. Teichert,
Copper(I)-Catalysed Transfer Hydrogenations with Ammonia Borane,
Chem Commun. 2017, 53, 732-735.
17.
N. O. Thiel and J. F. Teichert, Stereoselective alkyne semihydrogenations with an air-stable copper(I) catalyst,
Org. Biomol. Chem. 2016, 14, 10660-10666.
This work was highlighted in Synfacts 2017, 13, 57. and in Organic Chemistry Highlights.
16.
T. N. T. Nguyen, N. O. Thiel, F. Pape and J. F. Teichert,
Copper(I)-catalyzed Allylic Substitutions with a Hydride Nucleophile,
Org. Lett. 2016, 18, 2455-2458.
15.
F. Pape, N. O. Thiel and J. F. Teichert,
Z-Selective Copper(I)-catalyzed Alkyne Semihydrogenation with tethered Cu-alkoxide complexes,
Chem. Eur. J. 2015, 21, 15934-15938.
Highlighted in Nachr. Chem. 2016, 64, 279.
Before TU Berlin
14. | A. K. Schoonen, M. A. Fernández-Ibáñez, M. Fañanás-Mastral, J. F. Teichert, B. L. Feringa, Chiral amides via copper-catalysed enantioselective conjugate addition, Org. Biomol. Chem. 2014, 12, 36-41. This article was selected as an OBC hot article. |
13. | J. F. Teichert, D. Mazunin, J. W. Bode, Chemical Sensing of Polyols with Shapeshifting Boronic Acids as a Self-Contained Sensor Array, J. Am. Chem. Soc. 2013, 135, 11314 – 11321. This work was highlighted as a JACS Spotlight: J. Am. Chem. Soc. 2013, 135, 11679 and by Max von Delius in Nachrichten aus der Chemie 2014, 62, 522-525. |
12. | M. Fañanás-Mastral, J. F. Teichert, J. A. Fernández-Salas, D. Heijnen, B. L. Feringa, Enantioselective synthesis of Almorexant via Iridium-catalysed intramolecular allylic amidation, Org. Biomol. Chem. 2013, 11, 4521 – 4525. Highlighted in Synfacts, 2013, 9, 921. |
11. | K. K. Larson, M. He, J. F. Teichert, A. Naganawa, J. W. Bode, Chemical Sensing with Shapeshifting Organic Molecules, Chem. Sci. 2012, 3, 1825-1828. This work was highlighted by Stuart Cantrill in Nature Chemistry: Nature Chem. 2012, 4, 336-337. |
10. | J. F. Teichert, M. Fañanás-Mastral, B. L. Feringa, Synthetic approaches to highly functional β-carboline building blocks via allylic amidation, Synthesis 2012, 44, 409-416. |
9. | A. L. Gottumukkala, J. F. Teichert, D. Heijnen, N. Eisink, S. van Dijk, C. Ferrer, A. van den Hogenband, A. J. Minnaard, Pd-Diimine: A Highly Selective Catalyst System for the Base-Free Oxidative Heck Reaction, J. Org. Chem. 2011, 76, 3498-3501. Highlighted in Synfacts, 2011, 8, 894. |
8. | J. F. Teichert, T. den Hartog, M. Hanstein, C. Smit, B. ter Horst, V. Hernandez-Olmos, B. L. Feringa, A. J. Minnaard, Organocatalytic Reduction of Carbon-Carbon Double Bonds in Racemization-sensitive Compounds, ACS Catal. 2011, 1, 309-315. |
7. | J. F. Teichert, B. L. Feringa, Catalytic Asymmetric Conjugate Addition of Grignard Reagents to Coumarins – Synthesis of Versatile Chiral Building Blocks, Chem. Commun. 2011, 47, 2679-2681. Highlighted in Synfacts, 2011, 6, 642. |
6. | J. F. Teichert, M. Fañanás-Mastral, B. L. Feringa, Ir-catalyzed asymmetric allylic amidation – Enantioselective Synthesis of Chiral Tetrahydroisoquinolines, Angew. Chem. Int. Ed. 2011, 50, 688-691; Angew. Chem. 2011, 123, 714-717. Highlighted in Synfacts, 2011, 4, 419. |
5. | J. F. Teichert, S. Zhang, A. W. van Zijl, J. W. Slaa, A. J. Minnaard, B. L. Feringa, Cu-Catalyzed Asymmetric Allylic Alkylation in Combination with Ru-Catalyzed Metathesis: A Straightforward Approach to Chiral N-Heterocycles, Org. Lett. 2010, 12, 4658-4660. Highlighted in Synfacts, 2010, 12, 1392. |
4. | J. F. Teichert, B. L. Feringa, Catalytic Asymmetric Synthesis of 2,5-Naphthylpyrrolidine, Synthesis 2010, 7, 1200-1204. |
3. | J. F. Teichert, B. L. Feringa, Phosphoramidites – Privileged Ligands in Asymmetric Catalysis, Angew. Chem. Int. Ed. 2010, 49, 2486-2528; Angew. Chem. 2010, 122, 2538-2582. |
2. | J. F. Teichert, P. Oulié, K. Jacob, L. Vendier, M. Etienne, R. M. Claramunt, C. López, C. P. Medina, I. Alkorta, J. Elguéro, The strucutre of the Replacement of an H by a F Atom on the Supramolecular Structure of NH-Indazoles, New J. Chem. 2007, 31, 936-946. |
1. | P. Oulié, J. F. Teichert, L. Vendier, C. Dablemont, M. Etienne, Aromatic interactions in hydrotris(3-methylindazolyl)-borate organoniobium complexes: control of an alkyne ligand orientation in the crystal, New J. Chem. 2006, 30, 679-682. |