Inhalt des Dokuments
Es gibt keine deutsche Übersetzung dieser Webseite.
- © 2020 Thieme
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, accepted. DOI:
- © 2019 Wiley-VCH
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.
- © 2019 RSC
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.
- © 2019 Wiley-VCH
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.
- © 2019 Thieme
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.
- © 2019 RSC
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.
- © 2018 Wiley-VCH
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.
- © 2018 American Chemical Society
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.
- © 2017 Wiley-VCH
28.
J. F. Teichert,
Synthese im Blickpunkt: Benzol dearomatisieren mit Licht,
Nachr. Chem. 2017, 65, 1092-1095.
- © 2017 RSC
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.
- © 2017 Wiley-VCH
26.
F. Pape, J. F. Teichert,
Synthese im Blickpunkt: Polyketide am Fließband,
Nachr. Chem. 2017, 65, 879 - 883.
- © 2017 Wiley-VCH
25.
N. O. Thiel, J. F. Teichert,
Synthese im Blickpunkt: Interhalogenierung: Das Problemkind der Alkenbromierung,
Nachr. Chem. 2017, 65, 772 - 775.
- © 2017 Elsevier
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)
- © 2017 Wiley-VCH
23.
J. F. Teichert,
Synthese im Blickpunkt: Benachbarte Stereozentren unter voller Kontrolle,
Nachr. Chem. 2017, 65, 530 - 534.
- © 2017 American Chemical Society
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.
- © 2017 Wiley-VCH
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.
- © 2017 Thieme
20.
F. Pape, J. F. Teichert,
Tethered NHC Ligands for Stereoselective Alkyne Semihydrogenations,
Synthesis 2017, 49, 2470-2482.
- © 2017 Wiley-VCH
19.
J. F. Teichert,
Synthese im Blickpunkt: C-C Bindungen knüpfen mit Aktivestern,
Nachr. Chem. 2017, 65, 26-29.
- © 2016 RSC
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.
- © 2016 RSC
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.
- © 2016 American Chemical Society
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.
- © 2015 Wiley-VCH
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. |