Inhalt des Dokuments
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- © 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, accepted; ChemRXiv 2019, DOI: 10.26434/chemrxiv.9731279.v1
- © AK Teichert
33.
N. O. Thiel, B. Kaewmee, T. Tran Ngoc, J. F. Teichert,
A Simple Nickel Catalyst Enables Broad E-Selective Alkyne Semihydrogenation,
ChemRXiv 2019, DOI: 10.26434/chemrxiv.9715955.v1
- © 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. (Part of the Synlett Special Section 10th Young Investigators Workshop of the EuCheMS)
- © 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.
- © 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.
This work was highlighted in Synfacts 2018, 14, 1265 and in Nachr. Chem. 2018, 66, 943.
- © 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.
This work was highlighted in Synfacts 2018, 14, 161.
- © 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.
- © 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. |