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TU Berlin

Inhalt des Dokuments

Publications

Lupe

28.
J. F. Teichert,
Synthese im Blickpunkt: Benzol dearomatisieren mit Licht,
Nachr. Chem. 2017, 65, 1092 - 1095.

Lupe

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.

Lupe

26.
F. Pape, J. F. Teichert,
Synthese im Blickpunkt: Polyketide am Fließband,
Nachr. Chem. 2017, 65, 879 - 883.

Lupe

25.
N. O. Thiel, J. F. Teichert,
Synthese im Blickpunkt: Interhalogenierung: Das Problemkind der Alkenbromierung,
Nachr. Chem. 2017, 65, 772 - 775.

Lupe

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)

Lupe

23.
J. F. Teichert,
Synthese im Blickpunkt: Benachbarte Stereozentren unter voller Kontrolle,
Nachr. Chem. 2017, 65, 530 - 534
.

Lupe

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.

Lupe

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.

Lupe

20.
F. Pape, J. F. Teichert,
Tethered NHC Ligands for Stereoselective Alkyne Semihydrogenations,
Synthesis 2017, 49, 2470-2482.

Lupe

19.
J. F. Teichert,
Synthese im Blickpunkt: C-C Bindungen knüpfen mit Aktivestern,
Nachr. Chem. 2017, 65, 26-29.

Lupe

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.

Lupe

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.

Lupe

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.

Lupe

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.

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