SINCE 2014 AT RU BOCHUM
97.
Dominik L. Reinhard, Anna Schmidt, Marc Sons, Julian Wolf, Elric Engelage, Stefan M. Huber
Evaluating the halogen bonding strength of a iodoloisoxazolium (III) salt
Beilstein J. Org. Chem. 2024, 20, 241-2407. [PDF]
96.
Margarita Yanbaeva, Jan Soyka, Jana M. Holthoff, Philipp Rietch, Elric Engelage, Adrian ruff, Ute Resch-Genger, Robert Weiss, Siegfried Eigler, Stefan Matthias Huber
Dimethylene-Cyclopropanide Units as Building Blocks for Fluorescence Dyes.
Chem. Eur. J. 2024, e202402476. [Abstract] [PDF]
95.
Dragana Jovanovic, Meghana Polyodath Mohanan, Stefan M. Huber
Halogen, Chalcogen, Pnictogen, and Tretel Bonding in Non-Covalent Organocatalysis: An Update
Angew. Chem. Int. Ed. 2024, e202404823. [Abstract] [PDF]
Nichtkovalente Organokatalyse mit Halogen-, Chalkogen-, Pniktogen- und Tetrelbrücken: neuere Entwicklungen [PDF]
94.
Sercan Akbaba, Tim Steinke, Lukas Vogel, Elric Engelage, Mate Erdelyi*, Stefan Matthias Huber*
Elucidating the Bindinge Mode of Sulfur- and Selenium-Based Cationic Chalcogen-Bond Donors
Chem. Eur. J. 2024, 202400608. [Abstract] [PDF]
93.
Dominik L. Reinhard, Dana Kutzinski, Masihito Hatta, Elric Engelage, Stefan M. Huber*
Evaluation of a Bidentate 'Clamp' - Like Halogen-Bond Donor Motif Based on Iodonium (III) Moieties
Synlett. 2024, 35, 209-214. [Abstract] [Pdf]
92.
Christoph J. Vonnemann, David Bulfield, Elric Engelage, Stefan M. Huber*
A Halogen Bonding Molecular Tweezer
Org. Chem. Front., 2023, 10, 6146-6152. [Pdf]
91.
Dragana Jovanovic, Stefan M. Huber*
Cyclic Diaryliodonium Species as Synthetic Precursors and Halogen Bonding Organocatalysts
Chem. Rev. 2023, 123, 10527-10529. [Abstract] [Pdf]
90.
Dhananjoy Pal, Tim Steinke, Lukas Vogel, Elric Engelage, Sascha Heinrich, Dana Kutzinski, Stefan M. Huber*
A combined halogen- and chalcogen-bonding organocatalyst
Adv. Synth. Catal. 2023, 365, 2718-2723. (Special Issue: Iodine in Catalysis and Organic Synthesis) [Abstract] [Pdf]
89.
Julian Stoesser, Elric Engelage, Debora Belmonte, Stefan M. Huber*
Just at the limit: binding studies with neutral brominated terphenyl-derived halogen bond donors
CrystEngComm 2023, 25, 1501-1506. [Abstract] [Pdf]
88.
Tim Steinke, Elric Engelage, Stefan M. Huber*
Chalcogen bonding in the solid-state structures of 1,3-bis(benzimidazoliumyl)benzene-based chalcogen-bonding donors
Acta Cryst. C 2023, 79C, 26-35. (Part of a Special Collection on halogen, chalcogen, pnictogen and tetrel bonds). [Abstract] [Pdf]
87.
Raphaël Robidas, Dominik L. Reinhard, Stefan M. Huber,* Claude Y. Legault*
A Quantum-chemical Analysis on the Lewis Acidity of Diarylhalonium Ions
ChemPhysChem 2023, 24, e202200634. [Abstract] [Pdf]
86.
Jana M. Holthoff, Elric Engelage, Adrian Ruff, Laura Galazzo, Enrica Bordignon, Stefan M. Huber,* Robert Weiss*
A Potent Auto-Umpolung Ligand for Conjugative Radical Stabilization
Chem. Eur. J. 2023, 29, e202203149. [Abstract] [Pdf]
85.
Julian Stoesser, Elric Engelage, Stefan M. Huber*
Co-crystallization studies of the syn- and anti-atropisomers of triphenyl-based perfluorinated halogen bond donors with halides
CrystEngComm 2022, 24, 6974-6979. [Abstract] [Pdf]
84.
Raffaella Papagna, Dana Kutzinski, Stefan M. Huber*
Polymer-Bound Halogen Bonding Organocatalysis
Eur. J. Org. Chem. 2022, e202200852. [Abstract] [Pdf]
83.
Tim Steinke, Patrick Wonner, Richard M. Gauld, Sascha Heinrich, Stefan M. Huber*
Catalytic Activation of Imines by Chalcogen Bond Donors in a Povarov [4+2] Cycloaddition Reaction
Chem. Eur. J. 2022, 28, e202200917. (Part of a Special Collection on Noncovalent Interactions). [Abstract] [Pdf]
82.
Helgi Freyr Jónsson, Daniel Sethio, Julian Wolf, Stefan M. Huber, Anne Fiksdahl,* Mate Erdelyi*
Halogen Bond Activation in Gold Catalysis
ACS Catalysis 2022, 12, 7210-7220. [Abstract] [Pdf]
81.
Martin H. H. Völkel, Elric Engelage, Mykhailo Kondratiuk, Stefan M. Huber*
Evaluation of 6-halogenated 2-pyridone moieties as halogen bond donors
Eur. J. Org. Chem. 2022, e202200211. [Abstract] [Pdf]
80.
Naziha Tarannam, Martin H. H. Voelkel, Stefan M. Huber,* Sebastian Kozuch*
Chalcogen vs Halogen Bonding Catalysis in a Water-Bridge-Cocatalyzed Nitro-Michael Reaction
J. Org. Chem. 2022, 87, 1661–1668. [Abstract] [Pdf]
79.
Julian Stoesser,* Elric Engelage, Stefan M. Huber*
Synthesizing highly fluorinated oligophenyls via Negishi coupling of fluoroarylzinc pivalates
Synthesis 2022, 54, 711-722. [Abstract] [Pdf]
78. (Cooperation)
Mike Jörges, Alexander Kroll, Leif Kelling, Richard Gauld, Bert Mallick, Stefan M. Huber, Viktoria H. Gessner*
Synthesis, Crystal and Electronic Structures of a Thiophosphinoyl- and Amino-Substituted Metallated Ylide
ChemistryOpen 2021, 10, 1089-1094. [Abstract] [Pdf]
77. (Concept)
Jana Holthoff, Robert Weiss, Sergiy Rosokha,* Stefan M. Huber*
“Anti-electrostatic” halogen bonding between ions of like charge
Chem. Eur. J. 2021, 27, 16530-16542. [Abstract] [Pdf]
76.
Raphaël Robidas, Stefan M. Huber,* Claude Y. Legault*
Computational Investigation of Cyclic Substituted Iodine(III) Halogen Bond Donors
Arkivoc 2021, 2021, 128-140. [Abstract] [Pdf]
75. (Personal Account)
Raphaël Robidas, Dominik L. Reinhard, Claude Y. Legault,* Stefan M. Huber*
Iodine(III)-Based Halogen Bond Donors: Properties and Applications
Chem. Rec. 2021, 21, 1912-1927. [Abstract] [Pdf]
74.
Cody Loy, Jana M. Holthoff, Robert Weiss, Stefan M. Huber,* Sergiy Rosokha* “Anti-electrostatic” halogen bonding in solution
Chem. Sci. 2021, 12, 8246-8251. [Abstract] [Pdf]
73.
Elric Engelage, Hussein Hijazi, Martin Gartmann, Lise-Marie Chamoreau, Bernd Schöllhorn,* Stefan. M. Huber,* Claire Fave*
Towards redox-switchable organocatalysts based on bidentate halogen bond donors
Phys. Chem. Chem. Phys. 2021, 23, 4344 - 4352. [Abstract] [Pdf]
72.
Tim Steinke, Patrick Wonner, Elric Engelage, Stefan M. Huber*
Catalytic Activation of a Carbon-Chloride Bond by Dicationic Tellurium-Based Chalcogen Bond Donors
Synthesis 2021, 53, 2043-2050. (Invited Feature Article). [Abstract] [Pdf]
71.
Raphaël Robidas,* Claude Y. Legault, Stefan M. Huber
A low cost, high accuracy method for halogen bonding complexes
Phys. Chem. Chem. Phys. 2021, 23, 3041-3049. [Abstract] [Pdf]
70.
Revannath L. Sutar, Nikita Erochoka, Stefan M. Huber*
Mukaiyama aldol reaction catalyzed by (benz)imidazolium-based halogen bond donors
Org. Biomol. Chem. 2021, 19, 770-774. (Special Issue on halogen bonding in organic synthesis and catalysis). [Abstract] [Pdf]
previously posted on ChemRXiv (DOI: 10.26434/chemrxiv.12820652.v1)
69.
Dominik L. Reinhard, Flemming Heinen, Julian Stoesser, Elric Engelage, Stefan M. Huber*
Tuning the Halogen Bonding Strength of Cyclic Diaryliodonium Salts
Helv. Chim. Acta 2021, 104, e2000221. (Special Issue dedicated to the 65th birthday of Antonio Togni). [Abstract] [Pdf]
68.
Flemming Heinen, Dominik L. Reinhard, Elric Engelage, Stefan M. Huber*
A Bidentate Iodine(III)‐Based Halogen‐Bond Donor as a Powerful Organocatalyst
Angew. Chem. Int. Ed. 2021, 60, 5069-5073. [Abstract] [Pdf]
Ein zweizähniger Iod(III)‐basierter Halogenbrückendonor als leistungsfähiger Organokatalysator
Angew. Chem. 2021, 133, 5127-5132. [Abstract] [Pdf]
previously posted on ChemRXiv (DOI: 10.26434/chemrxiv.13019570.v1)
67. (Cooperation: DFT calculations)
Rajasekar Annapureddy, Finn Burg, Johannes Gramüller, Tino Golub, Christian Merten, Stefan M. Huber, Thorsten Bach*
Silver‐Catalyzed Enantioselective Sulfimidation Mediated by Hydrogen Bonding Interactions
Angew. Chem. Int. Ed. 2021, 60, 7920-7926. [Abstract] [Pdf]
Silver‐Catalyzed Enantioselective Sulfimidation Mediated by Hydrogen Bonding Interactions
Angew. Chem. 2021, 133, 7999-8005. [Abstract] [Pdf]
66.
Julian Wolf, Florian Huber, Nikita Erochok, Flemming Heinen, Vincent Guérin, Claude Legault,* Stefan F. Kirsch,* Stefan M. Huber*
Activation of a metal‐halogen bond by halogen bonding
Angew. Chem. Int. Ed. 2020, 59, 16496-16500. [Abstract] [Pdf]
Aktivierung einer Metall-Halogen-Bindung durch Halogenbrücken
Angew. Chem. 2020, 132, 16638-16643. [Abstract] [Pdf]
previously posted on ChemRXiv (DOI: 10.26434/chemrxiv.12107832.v1)
65.
Jana M. Holthoff, Elric Engelage, Robert Weiss,* Stefan M. Huber*
"Anti‐Electrostatic" Halogen Bonding
Angew. Chem. Int. Ed. 2020, 59, 11150-11157. [Abstract] [Pdf]
"Anti‐elektrostatische" Halogenbrücken
Angew. Chem. 2020, 132, 11244-11251. [Abstract] [Pdf]
previously posted on ChemRXiv (DOI: 10.26434/chemrxiv.11914884.v1)
64.
Flemming Heinen, Elric Engelage, Christopher J. Cramer, Stefan M. Huber*
Hypervalent Iodine(III) Compounds as Biaxial Halogen Bond Donors
J. Am. Chem. Soc. 2020, 142, 8633–8640. [Abstract] [Pdf]
63.
Revannath L. Sutar, E. Engelage R. Stoll, Stefan M. Huber*
Bidentate Chiral Bis(imidazolium)‐based Halogen Bond Donors: Synthesis and Applications in Enantioselective Recognition and Catalysis
Angew. Chem. Int. Ed. 2020, 59, 6806-6810. [Abstract] [Pdf]
Zweizähnige chirale Bis(imidazolium)‐basierte Halogenbrückendonoren: Synthese und Anwendungen in enantioselektiver Erkennung und Katalyse
Angew. Chem. 2020, 132, 6872-6877. [Abstract] [Pdf]
previously posted on ChemRXiv (DOI: 10.26434/chemrxiv.11371611.v1)
62.
Martin H. H. Voelkel, Patrick Wonner, Stefan M. Huber*
Preorganization: A Powerful Tool in Intermolecular Halogen Bonding in Solution
ChemistryOpen 2020, 9, 214-224. (Special Collection on Functional Supramolecular Systems, dedicated to Jean-Marie Lehn's 80th birthday). [Abstract] [Pdf]
61. (Cooperation: DFT calculations)
Franziska Pecho, You-Quan Zou, Johannes Grameller, Tadashi Mori, Stefan M. Huber, Andreas Bauer, Ruth M. Gschwind, Thorsten Bach*
A Thioxanthone Sensitizer with a Chiral Phosphoric Acid Binding Site: Properties and Applications in Visible Light‐Mediated Cycloadditions
Chem. Eur. J. 2020, 26, 5190-5194. [Abstract] [Pdf]
60.
Elric Engelage, Dominik Reinhard, Stefan M. Huber*
Is There a Single Ideal Parameter for Halogen‐Bonding‐Based Lewis Acidity?
Chem. Eur. J. 2020, 26, 3843-3861. [Abstract] [Pdf]
59.
David Bulfield,* Elric Engelage, Lucas Mancheski, Julian Stoesser, Stefan M. Huber*
Crystal Engineering with Multi‐Point Halogen Bonding: Double Two‐Point Donors and Acceptors at Work
Chem. Eur. J. 2020, 26, 1567-1575. [Abstract] [Pdf]
58.
Patrick Wonner, Tim Steinke, Lukas Vogel, Stefan M. Huber*
Carbonyl Activation by Selenium‐ and Tellurium‐based Chalcogen Bonding in a Michael Addition Reaction
Chem. Eur. J. 2020, 26, 1258-1262. [Abstract] [Pdf]
57.
Patrick Wonner, Alexander Dreger, Lukas Vogel, Elric Engelage, Stefan M. Huber*
Chalcogen Bonding Catalysis of a Nitro-Michael Reaction
Angew. Chem. Int. Ed. 2019, 58, 16923-16927. [Abstract] [Pdf]
Chalkogenbrückenkatalyse einer Nitro‐Michael‐Reaktion
Angew. Chem. 2019, 131, 17079-17083. [Abstract] [Pdf]
56. (Perspective)
Revannath L. Sutar,* Stefan M. Huber*
Catalysis of Organic Reactions through Halogen Bonding
ACS Catal. 2019, 9, 9622-9639. [Abstract] [Pdf]
55.
Patrick Wonner, Tim Steinke, Stefan M. Huber*
Activation of Quinolines by Cationic Chalcogen Bond Donors
Synlett 2019, 30, 1673-1678 (Cluster Issue: Organosulfur and Organoselenium Compounds in Catalysis). [Abstract] [Pdf]
54.
Jana M. Holthoff, Elric Engelage, Alexander B. Kowsari, Stefan M. Huber,* Robert Weiss*
Noble Metal Corrosion: Halogen Bonded Iodocarbenium Iodides Dissolve Elemental Gold--Direct Access to Gold-Carbene Complexes
Chem. Eur. J. 2019, 25, 7480-7484. [Abstract] [Pdf]
53.
Alexander Dreger, Patrick Wonner, Elric Engelage, Sebastian M. Walter, Raphael Stoll, Stefan M. Huber*
A halogen-bonding-catalysed Nazarov cyclisation reaction
Chem. Commun. 2019, 55, 8262-8265. [Abstract] [Pdf]
52. (Review)
Patrick Wonner, Lukas Vogel, Robert Weiss, Stefan M. Huber
Brücken mit Chalkogenen
Nachrichten aus der Chemie 10/2018, 952-956. [Abstract] [Pdf]
51. (Review)
Lukas Vogel, Patrick Wonner, Stefan M. Huber*
Chalcogen Bonding: An Overview
Angew. Chem. Int. Ed. 2018, 58, 1880-1891. [Abstract] [Pdf]
Chalkogenbrücken: eine Übersicht
Angew. Chem. 2018, 131, 1896-1907. [Abstract] [Pdf]
50.
Elric Engelage, Nils Schulz, Flemming Heinen, Stefan M. Huber,* Donald Truhlar,*
Christopher J. Cramer*
Refined SMD Parameters for Bromine and Iodine Accurately Model Halogen‐Bonding Interactions in Solution
Chem. Eur. J. 2018, 24, 15983-15987. [Abstract] [Pdf]
49.
Nils Schulz, Severin Schindler, Stefan M. Huber,* Mate Erdelyi*
NMR Determination of the Binding Constant of Ionic Species: A Caveat
J. Org. Chem. 2018, 83, 10881-10886. [Abstract] [Pdf]
48. (Cooperation: DFT calculations)
Nadine Zumbrägel, Christian Merten, Stefan M. Huber, Harald Gröger*
Enantioselective reduction of sulfur-containing cyclic imines through biocatalysis
Nat. Commun. 2018, 9, 1949-1957. [Abstract] [Pdf]
47.
Julian Stoesser, Gaspar Rojas, David Bulfield, Paulina I. Hidalgo, Jorge Pasán, Catalina Ruiz-Pérez, Claudio A. Jimenez*, Stefan M. Huber*
Halogen bonding two-point recognition with terphenyl derivatives
New. J. Chem. 2018, 42, 10476-10480. [Abstract] [Pdf]
46. (Highlight)
Patrick Wonner, Stefan M. Huber*
Selenverbindungen als Lewis-Säuren
GIT Labor-Fachzeitschrift 4/2018, 62-63.
Selenium-based Lewis Acids
GIT Laboratory Journal 4/2018, 24-25. [Abstract] [Pdf]
45.
Alexander Dreger, Elric Engelage, Bert Mallick, Paul D. Beer, Stefan M. Huber*
The role of charge in 1,2,3-triazol(ium)-based halogen bonding activators
Chem. Commun. 2018, 54, 4013-4016. [Abstract] [Pdf]
44.
Flemming Heinen, Elric Engelage, Alexander Dreger, Robert Weiss,* Stefan M. Huber*
Iod(III)-Derivate als Halogenbrücken-basierte Organokatalysatoren
Angew. Chem. 2018, 130, 3830-3833. [Abstract] [Pdf]
Iodine(III) derivatives as halogen bonding organocatalysts
Angew. Chem. Int. Ed. 2018, 57, 3892-3896. [Abstract] [Pdf]
43.
Nils Schulz, Pandian Sokkar, Elric Engelage, Severin Schindler, Mate Erdelyi, Elsa Sanchez-Garcia,* Stefan M. Huber*
XB, or not XB, that is the question: The Interaction Modes of Haloimidazolium Salts in Solution
Chem. Eur. J. 2018, 24, 3464-3473. [Abstract] [Pdf]
42.
Jonathan Thirman,* Elric Engelage, Stefan M. Huber, Martin Head-Gordon*
Probing the Interplay of Pauli Repulsion, Electrostatics, Dispersion and Charge Transfer in Halogen Bonding with Energy Decomposition Analysis
Phys. Chem. Chem. Phys. 2018, 20, 905-915. [Abstract] [Pdf]
41.
David Bulfield,* Stefan M. Huber*
Synthesis of Polyflourinated Biphenyls; Pushing the Boundaries of Suzuki–Miyaura Cross Coupling with Electron-Poor Substrates
J. Org. Chem. 2017, 82, 13188-13203. [Abstract] [Pdf]
40.
Jan-Philipp Gliese, Stefan H. Jungbauer, Stefan M. Huber*
A halogen-bonding-catalyzed Michael addition reaction
Chem. Commun. 2017, 53, 12052-12055. [Abstract] [Pdf]
39.
Patrick Wonner, Lukas Vogel, Florian Kniep, Stefan M. Huber*
Catalytic carbon-chlorine bond activation by selenium based chalcogen bond donors
Chem. Eur. J. 2017, 23, 16972-16975. [Abstract] [Pdf]
38.
Patrick Wonner, Lukas Vogel, Maximilian Düser, Luís Gomes, Florian Kniep, Bert Mallick, Daniel B. Werz, Stefan M. Huber*
Aktivierung einer Kohlenstoff-Halogen-Bindung durch selenbasierte Chalkogenbrücken
Angew. Chem. 2017, 129, 12172–12176. [Abstract] [Pdf]
Carbon–Halogen Bond Activation by Selenium-Based Chalcogen Bonding
Angew. Chem. Int. Ed. 2017, 56, 12009–12012. [Abstract] [Pdf]
37. (Review)
Stefan M. Huber*
Halogenbrücken in der Organokatalyse
Chem. Unserer Zeit 2017, 51, 37-39. [Abstract] [Pdf]
36. (Review)
Stefan M. Huber,* David Bulfield, Tatsuo Kaiho
Halogen Bond Donor Catalysis
Fine Chemicals 2016, 45, 42-52. [Article (in Japanese) available upon request.]
35. (Concept)
David Bulfield, Stefan M. Huber*
Halogen Bonding in Organic Synthesis and Organocatalysis
Chem. Eur. J. 2016, 22, 14434-14450. [Abstract] [Pdf]
34. (Author Profile)
Stefan M. Huber*
J. Phys. Org. Chem. 2016, 29, 4-5. [Abstract] [Pdf]
33.
Stefan H. Jungbauer, Stefan M. Huber*
Cationic multidentate halogen bond donors in halide abstraction organocatalysis: catalyst optimization by preorganization
J. Am. Chem. Soc. 2015, 137, 12110-12120. [Abstract] [Pdf]
32.
Stefan H. Jungbauer, Severin Schindler, Eberhardt Herdtweck, Sandro Keller,* Stefan M. Huber*
Multiple Multidentate Halogen Bonding in Solution, in the Solid State, and in the (Calculated) Gas Phase
Chem. Eur. J. 2015, 21, 13625-13636. [Abstract] [Pdf] // Corrigendum: [Pdf]
31.
Alexander Linke, Stefan H. Jungbauer, Stefan M. Huber,* Siegfried R. Waldvogel*
Potent affinity material for tracing acetone and related analytes based on molecular recognition by halogen bonds
Chem. Commun. 2015, 51, 2040-2043. [Abstract] [Pdf]
30. (Cooperation: DFT calculations)
James R. Frost, Stefan M. Huber, Stefan Breitenlechner, Christoph Bannwarth, Thorsten Bach*
Enantiotopos-selektive CH-Oxygenierung mit einem supramolekularen Ruthenium-Katalysator
Angew. Chem. 2015, 127, 701-705. [Abstract] [Pdf]
Enantiotopos-Selective CH Oxygenation Catalyzed by a Supramolecular Ruthenium Complex
Angew. Chem. Int. Ed. 2015, 54, 691-695. [Abstract] [Pdf]
29.
Stefan H. Jungbauer, David Bulfield, Florian Kniep, Christian W. Lehmann, Eberhardt Herdtweck, Stefan M. Huber*
Toward Molecular Recognition: Three-Point Halogen Bonding in the Solid State and in Solution
J. Am. Chem. Soc. 2014, 136, 16740-16743. [Abstract] [Pdf]
28.
Stefan H. Jungbauer, Sebastian M. Walter, Severin Schindler, Laxmidhar Rout, Florian Kniep, Stefan M. Huber*
Activation of a carbonyl compound by halogen bonding
Chem. Commun. 2014, 50, 6281-6284. [Abstract] [Pdf]
INDEPENDENT WORK AT TU MUNICH
27.
Riccardo Castelli, Severin Schindler, Sebastian M. Walter, Florian Kniep, Herman S. Overkleeft, Gijsbert A. Van der Marel, Stefan M. Huber,* Jeroen D. C. Codée*
Activation of Glycosyl Halides by Halogen Bonding
Chem. Asian J. 2014, 9, 2095-2098. [Abstract] [Pdf]
26. (Cooperation: DFT calculations)
Dominik Nitsch, Stefan M. Huber, Alexander Pöthig, Arjun Narayanan, George A. Olah, G. K. Surya Prakash, Thorsten Bach*
Chiral Propargylic Cations as Intermediates in SN1-Type Reactions: Substitution Pattern, Nuclear Magnetic Resonance Studies, and Origin of the Diastereoselectivity
J. Am. Chem. Soc. 2014, 136, 2851–2857. [Abstract] [Pdf]
25. (Account)
Stefan H. Jungbauer, Severin Schindler, Florian Kniep, Sebastian Walter, Laxmidhar Rout, Stefan M. Huber*
Multidentate Halogen-Bond Donors as Lewis Acidic Activators or Catalysts in
Halide Abstraction Reactions
Synlett 2013, 24, 2624-2628. [Abstract]
24. (Conference Report)
Anastassia N. Alexandrova,* Stefan M. Huber,* Ali Tavassoli*
The 3rd Transatlantic Frontiers in Chemistry Symposium
Chem. Eur. J. 2013, 19, 15777-15783. [Abstract] [Pdf]
23.
Florian Kniep, Stefan H. Jungbauer, Qi Zhang, Sebastian M. Walter, Severin Schindler, Ingo Schnapperelle, Eberhardt Herdtweck, Stefan M. Huber*
Organokatalyse mit neutralen multidentaten Halogenbrückendonoren
Angew. Chem. 2013, 125, 7166-7170. [Abstract] [Pdf]
Organocatalysis by Neutral Multidentate Halogen-Bond Donors
Angew. Chem. Int. Ed. 2013, 52, 7028-7032. [Abstract] [Pdf]
22.
Stefan M. Huber,* Joseph D. Scanlon, Elisa Jimenez-Izal, Jesus M. Ugalde, Ivan Infante*
On the directionality of halogen bonding
Phys. Chem. Chem. Phys. 2013, 15, 10350-10357. [Abstract] [Pdf]
21.
Sebastian M. Walter, Stefan H. Jungbauer, Florian Kniep, Severin Schindler, Eberhardt Herdtweck, Stefan M. Huber*
Perfluorinated versus cationic multidentate halogen-bond donors: A direct comparison
J. Fluorine Chem. 2013, 150, 14-20. [Abstract] [Pdf]
20.
Sebastian M. Walter, Mohammed G. Sarwar, Michael G. Chudzinski, Eberhardt Herdtweck, Alan J. Lough, Stefan M. Huber,* Mark S. Taylor*
Halogen bonding and pi-pi interactions in the solid state structure of a butadiynylene-linked bis(iodoperfluoroarene)
CrystEngComm 2013, 15, 3097-3101. [Abstract] [Pdf]
19.
Florian Kniep, Laxmidhar Rout, Sebastian M. Walter, Heide K. V. Bensch, Stefan H. Jungbauer, Eberhardt Herdtweck, Stefan M. Huber*
5-Iodo-1,2,3-triazolium-based multidentate halogen-bond donors as activating reagents
Chem. Commun. 2012, 48, 9299-9301. [Abstract] [Pdf]
18. (Cooperation: DFT calculations)
Anike Nörder, Sarah A. Warren, Eberhardt Herdtweck, Stefan M. Huber, Thorsten Bach*
Diastereotopos-Differentiation in the Rh-Catalyzed Amination of Benzylic Methylene Groups in the α-Position to a Stereogenic Center
J. Am. Chem. Soc. 2012, 134, 13524-13531. [Abstract] [Pdf]
17. (Cooperation: DFT calculations)
Philipp Fackler, Stefan M. Huber, Thorsten Bach*
Enantio- and Regioselective Epoxidation of Olefinic Double Bonds in Quinolones, Pyridones, and Amides Catalyzed by a Ruthenium Porphyrin Catalyst with a Hydrogen Bonding Site
J. Am. Chem. Soc. 2012, 134, 12869-12878. [Abstract] [Pdf]
16.
Stefan M. Huber,* Elisa Jimenez-Izal, Jesus M. Ugalde, Ivan Infante*
Unexpected Trends in Halogen-Bond Based Non-Covalent Adducts
Chem. Commun. 2012, 48, 7708-7710. [Abstract] [Pdf]
15.
Sebastian M. Walter, Florian Kniep, Laxmidhar Rout, Franz P. Schmidtchen, Eberhardt Herdtweck, Stefan M. Huber*
Isothermal Calorimetric Titrations on Charge-Assisted Halogen Bonds: Role of Entropy, Counterions, Solvent, and Temperature
J. Am. Chem. Soc. 2012, 134, 8507-8512. [Abstract] [Pdf]
14.
Florian Kniep, Sebastian M. Walter, Eberhardt Herdtweck, Stefan M. Huber*
4,4'-Azobis(halopyridinium) Derivatives: Strong Multidentate Halogen-Bond Donors with a Redox-Active Core
Chem. Eur. J. 2012, 18, 1306-1310. [Abstract] [Pdf]
13.
Sebastian M. Walter, Florian Kniep, Eberhardt Herdtweck, Stefan M. Huber*
Halogenbrücken-induzierte Aktivierung einer Kohlenstoff-Heteroatom-Bindung
Angew. Chem. 2011, 123, 7325-7329. [Abstract] [Pdf]
Halogen-Bond-Induced Activation of a Carbon-Heteroatom Bond
Angew. Chem. Int. Ed. 2011, 50, 7187-7191. [Abstract] [Pdf]
POSTDOC, PH.D. & DIPLOMA THESIS
12.
Stefan M. Huber,* Frank W. Heinemann, Pierre Audebert, Robert Weiss*
4,5-Bis(dialkylamino)-Substituted Imidazolium Systems: Facile Access to N-Heterocyclic Carbenes with Self-Umpolung Option
Chem. Eur. J. 2011, 17, 13078-13086. [Abstract] [Pdf]
11.
Harald Maid, Philipp Böhm, Stefan M. Huber, Walter Bauer, Werner Hummel, Nobert Jux, Harald Gröger*
Eisenkatalyse zur In-situ-Regenerierung oxidierter Co-faktoren durch Aktivierung und Reduktion von Sauerstoff: ein synthetisches Metalloporphyrin als biomimetische NAD(P)H-Oxidase
Angew. Chem. 2011, 123, 2445-2448. [Abstract] [Pdf]
Iron Catalysis for In Situ Regeneration of Oxidized Co-factors by Activation and Reduction of Molecular Oxygen: A Synthetic Metalloporphyrin as a Biomimetic NAD(P)H-Oxidase
Angew. Chem. Int. Ed. 2011, 50, 2397-2400. [Abstract] [Pdf]
10.
Stefan M. Huber, Abdul Rehaman M.S., Francesco Aquilante, Christopher J. Cramer,* Laura Gagliardi*
What Active Space Adequately Describes Oxygen Activation by a late Transition Metal? CASPT2 and RASPT2 Applied to Intermediates from the Reaction of Oxygen with a Cu(I)-alpha-Ketocarboxylate
J. Chem. Theory Comput. 2009, 5, 2967-2976. [Abstract] [Pdf]
9.
Thomas Riis-Johannessen, Natalia D. Favera, Tanya K. Todorova, Stefan M. Huber, Laura Gagliardi, Claude Piguet*
Understanding, Controlling and Programming Cooperativity in Self-assembled Polynuclear Complexes in Solution
Chem. Eur. J. 2009, 15, 12702-12718. [Abstract] [Pdf]
8.
Stefan M. Huber,* André Hennig, Frank G. Pühlhofer, Robert Weiss*
From DMF to isatine: A novel and general one-pot synthesis of isatine and its N-unsubstituted derivatives via nucleophilic substitution reactions on 1,2-bis-(dimethylamino)-1,2-dichloro-ethene
J. Heterocyclic Chem. 2009, 46, 421-427. [Abstract] [Pdf]
7.
Stefan M. Huber, Mehmed Z. Ertem, Francesco Aquilante, Laura Gagliardi,* William B. Tolman,* Christopher J. Cramer*
Generating CuII-Oxyl/CuIII-Oxo Species from Cu(I)-alpha-Ketocarboxylate Complexes and Dioxygen: In Silico Studies on Ligand Effects and C-H-Activation Reactivity
Chem. Eur. J. 2009, 15, 4886-4895. [Abstract] [Pdf]
6.
Itsik Bar-Nahum, Aalo K. Gupta, Stefan M. Huber, Mehmed Z. Ertem, Christopher J. Cramer,* William B. Tolman*
Reduction of Nitrous Oxide to Dinitrogen by a Mixed Valent Tricopper-Disulfido Cluster
J. Am. Chem. Soc. 2009, 131, 2812-2814. [Abstract] [Pdf]
5.
Robert Weiss,* Matthias Bess, Stefan M. Huber,* Frank W. Heinemann
Nucleophilic beta-Oniovinylation: Concept, Mechanism, Scope, and Applications
J. Am. Chem. Soc. 2008, 130, 4610-4617. [Abstract] [Pdf]
4.
Robert Weiss,* Frank G. Pühlhofer, Stefan M. Huber
Syntheses and Reactions of Polycationically Substituted Azido- and Diazidobenzenes
Eur. J. Org. Chem. 2007, 31, 5270-5276. [Abstract] [Pdf]
3.
Sungjun Hong, Stefan M. Huber, Laura Gagliardi, Christopher J. Cramer,* William B. Tolman*
Copper(I)-alpha-Ketocarboxylate Complexes: Characterization and Dioxygen Reactions That Yield Copper−Oxygen Intermediates Capable of Hydroxylating Arenes
J. Am. Chem. Soc. 2007, 129, 14190-14192. [Abstract] [Pdf]
2.
Robert Weiss,* Stefan M. Huber, Frank W. Heinemann, Pierre Audebert, Frank G. Pühlhofer
Struktur, Stereoelektronik und Synthesepotenzial von 1,2-Bisonio-1,2-bis(dialkylamino)ethenen
Angew. Chem. 2006, 118, 8228-8231. [Abstract] [Pdf]
Structure, Stereoelectronics, and Synthetic Potential of 1,2-Bisonio-1,2-bis(dialkylamino)ethenes
Angew. Chem. Int. Ed. 2006, 45, 8059-8062. [Abstract] [Pdf]
1.
Robert Weiss,* Stefan M. Huber, Frank G. Pühlhofer
Massive Electrostatic Effects on Heteropolar C-C Disconnections: Transforming a Phenyl Anion into a Potent Leaving Group
Eur. J. Org. Chem. 2005, 16, 3530-3535. [Abstract] [Pdf]
Edited by S. Huber
On the importance of halogen bonding in solution, demonstrating the specific advantages in various fields - from synthesis and catalysis to biochemistry and electrochemistry!
First published: 9 January 2021
Print ISBN:9783527347315 |Online ISBN:9783527825738
© 2021 Wiley‐VCH Verlag GmbH & Co. KGaA.
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1.
Severin Schindler, Stefan M. Huber*
Halogen Bonds in Organic Synthesis and Organocatalysis (p. 167-203)
in:
Pierangelo Metrangolo, Giuseppe Resnati (Eds.)
Halogen Bonding II: Impact on Materials Chemistry and Life Science
Topics in Current Chemistry, Vol. 359, Springer 2015. [Link]