Michael Göbel

ORCID: 0000-0002-5694-4823
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About
Contact & Profiles
Research Areas
  • RNA and protein synthesis mechanisms
  • DNA and Nucleic Acid Chemistry
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Chemical Synthesis and Analysis
  • Advanced biosensing and bioanalysis techniques
  • Crystallography and molecular interactions
  • Energetic Materials and Combustion
  • RNA Interference and Gene Delivery
  • Asymmetric Synthesis and Catalysis
  • Click Chemistry and Applications
  • Chemical Reaction Mechanisms
  • Molecular spectroscopy and chirality
  • Electron Spin Resonance Studies
  • Inorganic Fluorides and Related Compounds
  • Advanced Battery Materials and Technologies
  • Axial and Atropisomeric Chirality Synthesis
  • Carbohydrate Chemistry and Synthesis
  • Chemical Reactions and Mechanisms
  • Advancements in Battery Materials
  • Molecular Sensors and Ion Detection
  • RNA modifications and cancer
  • Thermal and Kinetic Analysis
  • Structural Analysis of Composite Materials
  • Lanthanide and Transition Metal Complexes

Goethe University Frankfurt
2014-2025

Leibniz Institute of Polymer Research
2014-2024

Robert Bosch (Germany)
2017

Leibniz Institute for Neurobiology
2014

Ludwig-Maximilians-Universität München
2006-2013

University of Maryland, College Park
2010

Energy Concepts (United States)
2010

Institut für Urheber- und Medienrecht
2009

Bauhaus-Universität Weimar
2009

University of Cambridge
2008

The first anionic tetrazole-2N-oxide has been prepared by mild aqueous oxidation of easily 5-nitrotetrazole with commercially available oxone in high yields. result protonating 5-nitrotetrazolate-2N-oxide identified as a hydroxytetrazole, and the nitrogen-rich salts including ammonium, hydroxylammonium, guanidinium, aminoguanidinum, diaminoguanidinium, triaminoguanidinium have characterized. When compared to nitrotetrazole, nitrotetrazole-2N-oxide show superior energetic performance...

10.1021/ja106892a article EN Journal of the American Chemical Society 2010-11-11

Abstract The development of new energetic materials is an emerging area chemistry facilitated by a worldwide need to replace used at present, due environmental considerations and safety requirements, while the same time securing high performance. such complex, owing fact that several different apparently mutually exclusive material properties have be met in order for become widely accepted. In turn, understanding basic principles structure property relationships highly desirable, as would...

10.1002/adfm.200801389 article EN Advanced Functional Materials 2009-01-12

Coordination or local environments (e.g., tetrahedra and octahedra) are powerful descriptors of the crystalline structure materials. These structural essential to understanding crystal chemistry design new However, extensive statistics on occurrence environment not available even common chemistries such as oxides. Here, we present first large-scale statistical analysis coordination cations in oxides using a large set experimentally observed compounds (about 8000). Using newly developed...

10.1021/acs.chemmater.7b02766 article EN Chemistry of Materials 2017-09-07

The correct target: cell division cycle protein 37 (Cdc37) and the heat shock (Hsp90) are molecular chaperones crucial for folding stabilization of kinases including oncogenic kinases. NMR studies show that celastrol, a recently identified triterpene targeting Hsp90, in fact binds to Cdc37 disrupts Cdc37–Hsp90 complex. Celastrol inactivates through thiol-mediated mechanism. Detailed facts importance specialist readers published as "Supporting Information". Such documents peer-reviewed, but...

10.1002/anie.200900929 article EN Angewandte Chemie International Edition 2009-07-10

SARS-CoV-2 contains a positive single-stranded RNA genome of approximately 30 000 nucleotides. Within this genome, 15 elements were identified as conserved between SARS-CoV and SARS-CoV-2. By nuclear magnetic resonance (NMR) spectroscopy, we previously determined that these fold independently, in line with data from vivo ex-vivo structural probing experiments. These contain non-base-paired regions potentially harbor ligand-binding pockets. Here, performed an NMR-based screening poised...

10.1002/anie.202103693 article EN cc-by Angewandte Chemie International Edition 2021-06-23

Why Pentose‐And Not Hexose‐Nucleic Acids? Part III. Oligo(2′,3′‐dideoxy‐β‐ D ‐glucopyranosyl)nucleotides. (‘Homo‐DNA’): Base‐Pairing Properties Summary in collaboration with Prof. Dr. C. E. Wintner , Haverford College, Haverford, PA 19041‐1392. The paper presents results of a comprehensive investigation on the pairing properties homo‐DNA oligonucleotides, preparation which has been described II this series [2]. was carried out by using established methods literature for characterization...

10.1002/hlca.19930760119 article EN Helvetica Chimica Acta 1993-02-10

Abstract 1,1‐Diamino‐2,2‐dinitroethene, C 2 H 4 N O (FOX‐7), is a novel high energy density material with low friction and impact sensitivity activation barrier to detonation. In this study, the previously unknown crystal structure of γ‐polymorph trimorphic FOX‐7 reported. γ‐FOX‐7 stable from ∼435 K until compound decomposes just above 504 K. A single α‐FOX‐7 ( P 1 /n, Z =4, =694.67(7) pm, b =668.87(9) c =1135.1(1) β=90.14(1)°, T =373 K) was first transformed into β‐FOX‐7 , =698.6(1)...

10.1002/prep.200700240 article EN Propellants Explosives Pyrotechnics 2007-12-01

Lithium–sulfur (Li–S) batteries hold a promising position as candidates for next-generation high-energy storage systems. Here, we combine inverse vulcanization of sulfur with multiwalled carbon nanotubes (MWCNTs) to increase the conductivity cathode materials Li–S batteries. The mixing process inversely vulcanized copolymer networks MWCNTs is aided by shear in two-roll mill take advantage soft nature copolymer. high-throughput method demands source conductive that can be intimately mixed S...

10.1021/acsami.3c09316 article EN ACS Applied Materials & Interfaces 2024-01-24

2-aminopyridine and 2-aminobenzimidazole were chosen as structural analogues to substitute guanidinium groups in receptor molecules designed phosphoryl transfer catalysts. Shifting the pKa of toward 7 was expected raise catalytic activities aqueous buffer. Although pKa's both heterocycles are similar (6.2 7.0), only led active RNA cleavers. All cleavage assays run with fluorescently labeled substrates a DNA sequencer. RNase contaminations would degrade enantioselectively. In contrast,...

10.1021/ja0443934 article EN Journal of the American Chemical Society 2005-01-27

[reaction: see text] Enantioselective catalysis of Diels-Alder reactions is mostly achieved by coordinating the dienophile to relatively strong chiral Lewis acids. Here we report on a novel approach employing hydrogen-bond-mediated association dienophiles host molecules. In reaction forming steroid skeleton norgestrel, amidinium ions induce 5:ent-5 ratios up 2.5:1. Improved and simplified catalysts may become interesting candidates perform stereoselective transformations.

10.1021/ol991276i article EN Organic Letters 2000-01-01

Why Pentose and Not Hexose Nucleic Acids? Part II . Preparation of Oligonucleotides Containing 2′,3′‐Dideoxy‐β‐ D ‐glucopyranosyl Building Blocks (7) This paper describes the preparation 2′,3′‐dideoxy‐β‐ ‐glucopyranosyl‐( = ‐ erythro ‐hexopyranosyl)‐derived nucleosides five bases adenine, cytosine, guanine, thymine, uracil ( ‘homo‐de‐oxyribonucleosides’) as well synthesis oligonucleotides derived from them. The methods used for both nucleoside oligonucleotide closely follow known in...

10.1002/hlca.19920750503 article EN Helvetica Chimica Acta 1992-08-13

Abstract Energetic salts containing the nitroformate (trinitromethanide) anion with several nitrogen‐rich cations were investigated, including ammonium (ANF), melaminium (MNF), guanidinium monohydrate (GNFH), aminoguanidinium (AGNF), diaminoguanidinium (DAGNF) as well triaminoguanidinium (TAGNF). All characterized using vibrational spectroscopy (IR, Raman), mass spectrometry, multinuclear NMR and elemental analysis. The thermal decomposition of was monitored differential scanning...

10.1002/zaac.200700114 article EN Zeitschrift für anorganische und allgemeine Chemie 2007-04-23

Hydrazoic acid (HN(3))--potentially explosive, highly toxic, and very hygroscopic--is the simplest covalent azide contains 97.7 wt % nitrogen. Although its molecular structure was established decades ago, crystal has now been solved by X-ray diffraction for first time. Molecules of HN(3) are connected to each other hydrogen bonds in nearly planar layers parallel (001) with stacking sequence A, B, ... The layer distance, at 2.950(1) Å, is shorter than that 2H-graphite [3.355(2) Å]. N-H···N...

10.1021/ja2027053 article EN Journal of the American Chemical Society 2011-06-24

Proximity effects and electrophilic activation combined account for the accelerated ring-opening in transesterification of 1 with amidinium alcohol 2. The spatial proximity arise a contact ion-pair Electrophilic causes 9000-fold rate enhancement reaction 2 relative to phenylalcohol; addition phenyl form 3 caused 25-fold increase.

10.1002/anie.199202071 article EN Angewandte Chemie International Edition 1992-02-01

RNA cleaving tris(2-aminobenzimidazoles) have been attached to DNA oligonucleotides via disulfide or amide bonds. The resulting conjugates are effective organocatalytic nucleases showing substrate and site selectivity as well saturation kinetics. benzimidazole also degrade enantiomeric RNA. This observation rules out contamination effects an alternative explanation of degradation. pH dependency shows that the catalyst is most active in deprotonated state. Typical half-lifes substrates range...

10.1021/ja061036f article EN Journal of the American Chemical Society 2006-05-25

The heptapeptide H-Iva-Api-Iva-ATANP-Iva-Api-Iva-NHCH 3 (P1a), where Iva is (S)-isovaline, Api 4-amino-4-carboxypiperidine, and ATANP (S)-2-amino-3-[1-(1,4,7-triazacyclononane)]propanoic acid, has been synthesized. Its conformation in aqueous solution essentially that of a 10 -helix. By connecting three copies P1a to functionalized Tris(2-aminoethyl)amine (Tren) platform new peptide template, [T(P1) ], was obtained. This molecule able bind up four metal ions (Cu II or Zn ): one the Tren...

10.1073/pnas.072642699 article EN Proceedings of the National Academy of Sciences 2002-04-09

Spin labeling of oligonucleotides with nitroxides is hampered by their intrinsic instability under conditions solid‐phase synthesis and enzymatic ligation. Although nitroxide decomposition can be avoided in some cases postsynthetic introduction or special reaction conditions, a more general solution would reversible protection the radical. We have recently developed such method based on photolabile groups for DNA demonstrated application EPR spectroscopy. Here, we extend this to RNA...

10.1002/ejoc.201601174 article EN European Journal of Organic Chemistry 2016-12-28

Rates never before achieved for the hydrolysis of amides are attained by Cu2(O2) complex 1, which converts dimethylformamide into formate ion in seconds (half-lives water often several years!). The interacting Cu ions play an important role. Such simple model systems can provide insights structure–activity relationships enzymes and even lead to development highly active catalysts.

10.1002/anie.199411411 article EN Angewandte Chemie International Edition 1994-06-22

Amidines and guanidines are important functional groups in molecular recognition host-guest chemistry. Here it is shown that lipophilic amidinium ions catalyze a cycloaddition reaction representing the key step of Quinkert-Dane estrone synthesis. Hydrogen-bond-mediated association with organic cation leads to an electrophilic activation dienophile enhanced rates Diels-Alder reaction. The observed effects similar those expected from mild Lewis acids. In competition experiments, catalysis...

10.1021/jo991372x article EN The Journal of Organic Chemistry 2000-02-24

We describe in full the first synthesis of potent insect antifeedant azadirachtin through a highly convergent approach. An O-alkylation reaction is used to unite decalin ketone and propargylic mesylate fragments, after which Claisen rearrangement constructs central C8-C14 bond stereoselective fashion. The allene results from this sequence then enables second critical carbon-carbon forming event whereby [3.2.1] bicyclic system, present natural product, generated via 5-exo-radical cyclisation...

10.1002/chem.200801103 article EN Chemistry - A European Journal 2008-09-26

Starting from Dane's diene and methylcyclopentenedione, (+)-estrone is synthesized along the Quinkert−Dane route in 24% total yield. The key step an enantioselective Diels−Alder reaction promoted by amidinium catalyst as efficiently a traditional Ti-TADDOLate Lewis acid.

10.1021/jo100053j article EN publisher-specific-oa The Journal of Organic Chemistry 2010-03-19
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