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Profil bibliographique

Stefan M. Huber

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

341Publications signalées
9510Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Crystallization and Solubility StudiesX-ray Diffraction in CrystallographyCrystallography and molecular interactionsAsymmetric Synthesis and CatalysisFluorine in Organic Chemistry

Les publications récentes

Accès ouvert 2026 article OpenAlex

Open‐Shell Tetra(dicyanomethylene)‐bicyclopropenylidene CN8CP2 Radical Anion as Strong Electron Acceptor

Jan Soyka, Margarita Yanbaeva, Niklas Limberg, Alok Mahata et autres

We report the synthesis, structural characterization, and optoelectronic properties of a highly electron‐deficient bi(cyclopropylidene)‐framework ( CN8CP2 ). The developed one‐pot synthesis gives access to the dianionic species via thermally induced homocoupling of an iodinated precursor. The controlled oxidation yields the radical anion, …

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0 citations ChemistryEurope
Accès ouvert 2026 article OpenAlex

Self‐Complementary Dimers Based on Zwitterionic Halogen Bond Donors

Dana Kutzinski, Raffaella Papagna, Elric Engelage, Lianne H E Wieske et autres

Even though halogen bonding is routinely used in crystal engineering and beyond, motifs offering multipoint interactions are still rare. This applies in particular to self-complementary systems which incorporate both halogen bond donating and accepting moieties. In this study, we present the first …

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0 citations Chemistry - A European Journal
Accès ouvert 2025 article OpenAlex

Enantioselective Intramolecular C–H Alkylation Catalyzed by a Nonsymmetric Chiral Cobalt Porphyrin

Christoph Buchelt, Stefan Breitenlechner, Julian Zuber, Stefan M. Huber et autres

High Resolution Image Download MS PowerPoint Slide Upon catalysis (1 mol %) by a chiral cobalt porphyrin, quinazolinones with a tethered diazo alkane precursor underwent an enantioselective C–H alkylation at carbon atom C4. Formation of five-, six-, and seven-membered rings was successfully …

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2 citations Journal of the American Chemical Society
2025 other OpenAlex

Synthetic Transformations Assisted by Halogen, Chalcogen, and Pnictogen Bonding

Meghana Poliyodath Mohanan, Dragana Jovanovic, Stefan M. Huber

This chapter provides an overview and covers key advancements of noncovalent organocatalysis with interactions based on electrophilic halogen, chalcogen and pnictogen centers. While the focus is on the latest trends, a short introduction on earlier studies is also provided for each interaction. …

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0 citations
Accès ouvert 2025 article OpenAlex

Ortho ‐Carborane‐Derived Halogen‐Bonded Sandwich Complexes

Christoph J. Vonnemann, Elric Engelage, Jas S. Ward, Kari Rissanen et autres

We recently introduced multidentate halogen-bonding receptors based on C-iodinated ortho-Carborane moieties. Following up on our results in solution, which indicated a second binding event for sub-stochiometric concentrations of halide guests, we herein present a systematic co-crystallization study with halides to further evaluate …

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1 citation Chemistry - A European Journal
Accès ouvert 2025 preprint OpenAlex

Biaxial Recognition: Towards Chiral Resolution of Allene-Dicarbonyl Compounds by Iodolium-Based Halogen Bond Donors

Anna Schmidt, Dominik L. Reinhard, Elric Engelage, Stefan M. Huber

The coordination of allene dicarbonyl compounds to cyclic iodonium salts is presented as a new biaxial halogen bonding recognition motif. 1H¬ NMR titrations and isothermal titration calorimetry (ITC) of such adducts were performed, resulting in a binding constant as high as 6.9·10^5 …

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0 citations ChemRxiv
2025 article OpenAlex

Halogen Bonding in Solution: Under Pressure

Saber Mehrparvar, Marcel Klinksiek, Richard M. Gauld, Julian Wolf et autres

The first study of the high-pressure behavior of organic halogen bond donors in solution is presented: HP-NMR titrations were performed in various solvents, primarily with a neutral tridentate halogen bond donor and an orthoamide or halides as Lewis bases. While the orthoamide …

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4 citations Journal of the American Chemical Society
Accès ouvert 2025 article OpenAlex

Highly Enantioselective Organocatalysis with Bidentate Halogen Bond Donors

Julian Wolf, Meghana Poliyodath Mohanan, Raphaël Robidas, Revannath L. Sutar et autres

As the employment of "non-classical" non-covalent interactions like halogen bonding (XB) in asymmetric catalysis is still at a very early stage, there are significant challenges to overcome. In some reported cases, the relevance of halogen bonding to the catalytic action is unclear, …

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12 citations Angewandte Chemie International Edition
Accès ouvert 2025 article OpenAlex

Hochgradig enantioselektive Organokatalyse mit zweizähnigen Halogenbrückendonoren

Julian Wolf, Meghana Poliyodath Mohanan, Raphaël Robidas, Revannath L. Sutar et autres

Zusammenfassung Da sich der Einsatz „nicht‐klassischer“ nicht‐kovalenter Wechselwirkungen wie der Halogenbrücken (XB) in der asymmetrischen Katalyse noch in einem sehr frühen Stadium befindet, gibt es noch erhebliche Herausforderungen zu überwinden. In einigen berichteten Beispielen ist die Bedeutung der Halogenbrücken für die katalytische …

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0 citations Angewandte Chemie
Accès ouvert 2025 article OpenAlex

Asymmetric Counteranion-Directed Halogen Bonding Catalysis

Dominik L. Reinhard, Anna Iniutina, Sven Reese, T. Shaw et autres

High Resolution Image Download MS PowerPoint Slide Halogen bonding has been established as a promising tool in organocatalysis. Asymmetric processes are nevertheless scarce, and their applications are limited to a few studies applying chiral halogen bond donors. Herein, we combine halogen bonding …

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26 citations Journal of the American Chemical Society
Accès ouvert 2025 article OpenAlex

Ortho ‐Carborane‐Derived Halogen Bonding Organocatalysts

Christoph J. Vonnemann, Elric Engelage, Jas S. Ward, Kari Rissanen et autres

Abstract Multidentate neutral halogen bonding catalysts based on iodinated icosahedral ortho ‐carborane moieties are introduced. Co‐crystallization‐studies, calorimetric measurements, and 1 H NMR titrations demonstrate their strong binding to halides and neutral compounds, further underlined by quantum‐chemical calculations. Thus, their superior Lewis acidity …

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13 citations Angewandte Chemie International Edition
Accès ouvert 2025 article OpenAlex

Ortho ‐Carborane‐Derived Halogen Bonding Organocatalysts

Christoph J. Vonnemann, Elric Engelage, Jas S. Ward, Kari Rissanen et autres

Abstract Multidentate neutral halogen bonding catalysts based on iodinated icosahedral ortho ‐carborane moieties are introduced. Co‐crystallization‐studies, calorimetric measurements, and 1 H NMR titrations demonstrate their strong binding to halides and neutral compounds, further underlined by quantum‐chemical calculations. Thus, their superior Lewis acidity …

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1 citation Angewandte Chemie

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