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Inhalt des Dokuments

Publications

Lupe [1]

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 [2]2019, DOI: 10.26434/chemrxiv.9731279.v1 [3]

Lupe [4]

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 [5]

Lupe [6]

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 [7]. (Part of the Synlett Special Section 10th Young Investigators Workshop of the EuCheMS)

Lupe [8]

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.

Lupe [9]

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 [10].

Lupe [11]

29.
M. Das, T. Kaicharla, J. F. Teichert,
Stereoselective Alkyne Hydrohalogenation by Trapping of Transfer Hydrogenation Intermediates,
Org. Lett. 2018, 20, 4926 [12]. This work was highlighted in Synfacts 2018, 14, 1265 [13] and in Nachr. Chem. 2018, 66, 943 [14].

Lupe [15]

28.
J. F. Teichert,
Synthese im Blickpunkt: Benzol dearomatisieren mit Licht,
Nachr. Chem. 2017, 65, 1092 - 1095 [16].

Lupe [17]

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 [18].

Lupe [19]

26.
F. Pape, J. F. Teichert,
Synthese im Blickpunkt: Polyketide am Fließband,
Nachr. Chem. 2017, 65, 879 - 883 [20].

Lupe [21]

25.
N. O. Thiel, J. F. Teichert,
Synthese im Blickpunkt: Interhalogenierung: Das Problemkind der Alkenbromierung,
Nachr. Chem. 2017, 65, 772 - 775 [22].

Lupe [23]

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 [24].
(
Invited manuscript for the Symposium-in-Print on the occasion of the Tetrahedron Prize 2017 for Ben Feringa)

Lupe [25]

23.
J. F. Teichert,
Synthese im Blickpunkt: Benachbarte Stereozentren unter voller Kontrolle,
Nachr. Chem. 2017, 65, 530 - 534 [26].

Lupe [27]

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 [28].

Lupe [29]

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 [30].

Lupe [31]

20.
F. Pape, J. F. Teichert,
Tethered NHC Ligands for Stereoselective Alkyne Semihydrogenations,
Synthesis 2017, 49, 2470-2482 [32].

Lupe [33]

19.
J. F. Teichert,
Synthese im Blickpunkt: C-C Bindungen knüpfen mit Aktivestern,
Nachr. Chem. 2017, 65, 26-29 [34].

Lupe [35]

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 [36]

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 [37].

Lupe [38]

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.
[39]

Lupe [40]

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. [41]
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 [42].
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 [43].
This work was highlighted as a JACS Spotlight: J. Am. Chem. Soc. 2013, 135, 11679 [44] and by Max von Delius in Nachrichten aus der Chemie 2014, 62, 522-525. [45]

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 [46].
Highlighted in Synfacts, 2013, 9, 921 [47].

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 [48].
This work was highlighted by Stuart Cantrill in Nature Chemistry: Nature Chem. 2012, 4, 336-337 [49].
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 [50].

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 [51].
Highlighted in Synfacts, 2011, 8, 894 [52].

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 [53].

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 [54].
Highlighted in Synfacts, 2011, 6, 642 [55].

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 [56]; Angew. Chem. 2011, 123, 714-717 [57].
Highlighted in Synfacts, 2011, 4, 419 [58].

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 [59].
Highlighted in Synfacts, 2010, 12, 1392 [60].

4.
J. F. Teichert, B. L. Feringa, 
Catalytic Asymmetric Synthesis of 2,5-Naphthylpyrrolidine,
Synthesis 2010, 7, 1200-1204 [61].

3.
J. F. Teichert, B. L. Feringa, 
Phosphoramidites – Privileged Ligands in Asymmetric Catalysis,
Angew. Chem. Int. Ed. 2010, 49, 2486-2528 [62]; Angew. Chem. 2010, 122, 2538-2582 [63].

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 [64].

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 [65].

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