Matthias A. Schade

ORCID: 0000-0001-6283-0470
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Research Areas
  • Coordination Chemistry and Organometallics
  • Catalytic Cross-Coupling Reactions
  • Asymmetric Synthesis and Catalysis
  • Catalytic C–H Functionalization Methods
  • Chemical synthesis and alkaloids
  • RNA and protein synthesis mechanisms
  • Influenza Virus Research Studies
  • Viral Infections and Vectors
  • Advanced Synthetic Organic Chemistry
  • Cyclopropane Reaction Mechanisms
  • Respiratory viral infections research
  • Fire effects on ecosystems
  • Synthesis of heterocyclic compounds
  • Viral Infections and Outbreaks Research
  • Synthetic Organic Chemistry Methods
  • Organoboron and organosilicon chemistry
  • RNA Interference and Gene Delivery
  • Bacteriophages and microbial interactions
  • Catalytic Alkyne Reactions
  • interferon and immune responses
  • Peptidase Inhibition and Analysis
  • Chemical Synthesis and Analysis
  • Herpesvirus Infections and Treatments
  • Viral Infections and Immunology Research
  • DNA and Nucleic Acid Chemistry

Humboldt-Universität zu Berlin
2012-2024

Leibniz Institute of Environmental Medicine
2023-2024

Ludwig-Maximilians-Universität München
2006-2014

Universidad de Málaga
2008

Abstract The presence of LiCl considerably facilitates the insertion magnesium into various aromatic and heterocyclic bromides. Several functional groups, such as ‐OBoc, ‐OTs, ‐Cl, ‐F, ‐CF 3 , ‐OMe, ‐NMe 2 ‐N NR are well tolerated. a cyano group leads in some cases to competitive reduction organic halide corresponding ArH compound. sensitive groups methyl or ethyl ester is tolerated upon situ trapping intermediate reagent with ZnCl . This method can also be applied preparation functionalized...

10.1002/chem.200900575 article EN Chemistry - A European Journal 2009-06-19

In the presence of zinc dust (1.5-2.0 equiv) and LiCl equiv), various benzylic chlorides bearing functional groups (iodide, cyanide, ester, ketone) are smoothly converted at 25 degrees C to corresponding reagents without homo-coupling (<5%). The utility these is demonstrated by a short synthesis papaverine.

10.1021/ol7030697 article EN Organic Letters 2008-02-21

Organocopper compounds prepared by the transmetalation of functionalized arylmagnesium halides with CuCN·2LiCl undergo smooth cross-coupling reactions aryl fluorides and tosylates bearing a carbonyl function in ortho position presence Co(acac)2 (7.5 mol %), Bu4NI (1 equiv), 4-fluorostyrene (20 %) as promoters DME/THF/DMPU leading to polyfunctional aromatics or heterocycles.

10.1021/ol0529142 article EN Organic Letters 2006-01-14

A wide range of polyfunctional aryl, heteroaryl, alkyl, and benzylic zinc reagents were coupled with unsaturated halides bearing an acidic NH or OH function, using Pd(OAc)(2) (1 mol %) S-Phos (2 as catalyst without the need protecting groups.

10.1021/ol8009013 article EN Organic Letters 2008-06-05

A wide range of polyfunctional aryl, heteroaryl, alkyl, and benzylic zinc reagents were coupled with unsaturated aryl halides bearing an acidic NH or OH proton, using Pd(OAc)2 (1 mol %) S-Phos (2 as catalyst without the need protecting groups. similar nickel-catalyzed reaction is described. The relative kinetic basicity organozinc compounds well their stability toward protons also

10.1021/jo8015852 article EN The Journal of Organic Chemistry 2008-10-04

Organic iodides bearing a cationic quaternary ammonium group at remote position react with zerovalent Pd complexes, Zn, or In leading to C−I bond insertion. The resulting charge-tagged organometallics can be detected by electrospray-ionization mass spectrometry, which provides detailed information on their stoichiometry, oxidation state, and coordination sphere. properties of the observed organopalladium -zinc intermediates largely agree previous findings, whereas organoindium species show...

10.1021/jo101337a article EN The Journal of Organic Chemistry 2010-09-13

Benzylic zinc reagents prepared by direct insertion of to benzylic chlorides in the presence LiCl undergo smooth cross-coupling reactions with aromatic chlorides, bromides and tosylates using Ni(acac)2 PPh3 as a catalyst system.

10.1039/b803072c article EN Chemical Communications 2008-01-01

In this review we summarize the most important procedures for preparation of functionalized organzinc and organomagnesium reagents. addition, new methods polyfunctional aryl- heteroaryl zinc- magnesium compounds, as well Pd-catalyzed cross-coupling reactions, are reported herein. Experimental details given reactions in Supporting Information File 1 article.

10.3762/bjoc.7.147 article EN cc-by Beilstein Journal of Organic Chemistry 2011-09-13

Abstract The genome of influenza A viruses (IAV) is encoded in eight distinct viral ribonucleoproteins (vRNPs) that consist negative sense RNA (vRNA) covered by the IAV nucleoprotein. Previous studies strongly support a selective packaging model which vRNP segments are bundling to an octameric complex, integrated into budding virions. However, pathway(s) generating complete bundle not known. We here use multiplexed FISH assay monitor all vRNAs parallel human lung epithelial cells. Analysis...

10.1038/s41467-020-18108-1 article EN cc-by Nature Communications 2020-08-28

Organozinc halides, which are prepared either by direct zinc insertion or halogen−magnesium exchange and subsequent transmetalation with ZnCl2, react smoothly commercially available trichloroacetyl isocyanate to give, after hydrolysis, the corresponding primary amides. This method is compatible a variety of functional groups such as an ester cyano group. Also heterocyclic-, alkenyl, acetylenic reagents converted amides under these conditions.

10.1021/ol101469f article EN Organic Letters 2010-07-22

Highly functionalized cyclic and acyclic alkenylzinc reagents bearing functional groups such as aldehyde, keto, ester were readily prepared by either direct zinc insertion in the presence of LiCl or magnesium ZnCl2. Subsequent functionalization reactions, Negishi cross-couplings, acylations, allylations, furnished polyfunctional compounds excellent yields. As a service to our authors readers, this journal provides supporting information supplied authors. Such materials are peer reviewed may...

10.1002/anie.201302058 article EN Angewandte Chemie International Edition 2013-05-10

Lateral partitioning of lipid-modified molecules between liquid-disordered (ld) and liquid-ordered (lo) domains depends on the type lipid modification, presence a spacer, membrane composition, temperature. Here, we show that lo domain palmitoylated peptide nucleic acid (PNA) can be influenced by formation four-component complex with ld tocopherol-modified DNA: PNA-DNA partitioned into domains. Enzymatic cleavage DNA linker led to disruption restored initial distribution lipophilic acids...

10.1021/ja309256t article EN Journal of the American Chemical Society 2012-11-19

A new method for the preparation of highly functionalized benzylic zinc chlorides by direct insertion dust into corresponding in presence LiCl is described without formation homocoupling products (<5 %). Various reactions these reagents with a broad range electrophiles, which lead to polyfunctionalized products, are reported. In particular, cross-coupling aromatic chlorides, bromides, and tosylates [Ni(acac)(2)] (acac=acetylacetonate) PPh(3) proceeded good excellent yields give diaryl...

10.1002/asia.200800161 article EN Chemistry - An Asian Journal 2008-07-05

Abstract Readily available 1,1‐dichloro‐2‐alkynes are versatile starting materials for the synthesis of polyfunctionalized allenes. They can be prepared from commercially terminal alkynes in a two‐step procedure. The Cu‐mediated reaction several 1,1‐propargylic derivatives with functionalized alkyl, benzylic, or allylic zinc reagents proceeds exclusively S N 2′ selectivity and allows rapid efficient chloroallenes. These chloroallenes undergo novel Cu I ‐catalyzed substitution arylmagnesium...

10.1002/chem.201003273 article EN Chemistry - A European Journal 2011-03-07

The family Hantaviridae comprises a diverse group of virus species and is considered an emerging global public health threat. Individual hantavirus differ considerably in terms their pathogenicity but also cell biology host-pathogen interactions. In this study, we focused on the most prevalent pathogenic Europe, Puumala (PUUV), investigated entry internalization PUUV into mammalian cells. We show that both clathrin-mediated endocytosis macropinocytosis are cellular pathways exploited by to...

10.1128/jvi.00184-20 article EN Journal of Virology 2020-04-29

ABSTRACT Infected peripheral blood mononuclear cells (PBMC) effectively transport equine herpesvirus type 1 (EHV-1), but not EHV-4, to endothelial (EC) lining the vessels of pregnant uterus or central nervous system, a process that can result in abortion myeloencephalopathy. We examined, using dynamic vitro model, differences between EHV-1 and EHV-4 infection PBMC PBMC-EC interactions. In order evaluate viral transfer infected EC, cocultivation assays were performed. Only was transferred...

10.1128/jvi.01809-15 article EN Journal of Virology 2015-09-17

Abstract Hantavirus assembly and budding are governed by the surface glycoproteins Gn Gc. In this study, we investigated of Puumala, most abundant species in Europe, using fluorescently labeled wild-type constructs cytoplasmic tail (CT) mutants. We analyzed their intracellular distribution, co-localization oligomerization, applying comprehensive live, single-cell fluorescence techniques, including confocal microscopy, imaging flow cytometry, anisotropy Number&amp;Brightness analysis....

10.1038/s41598-018-36879-y article EN cc-by Scientific Reports 2019-01-24

Hoch funktionalisierte cyclische und acyclische Alkenylzinkreagentien mit Aldehyd-, Keto- oder Estergruppen können einfach durch direkte Zn-Insertion in Gegenwart von LiCl Mg-Insertion ZnCl2 hergestellt werden. Mehrfach Produkte wurden nachfolgende Funktionalisierungsreaktionen wie Negishi-Kreuzkupplungen, Acylierungen Allylierungen exzellenten Ausbeuten erhalten. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are...

10.1002/ange.201302058 article EN Angewandte Chemie 2013-05-10

The influenza A virus (IAV) genome is segmented into eight viral ribonucleoproteins, each expressing a negatively oriented RNA (vRNA). Along the infection cycle, highly abundant single-stranded small RNAs (svRNA) are transcribed in segment-specific manner. sequences of svRNAs and vRNA 5'-ends identical conserved among all IAV strains. Here, we demonstrate that these can be used as target for pan-selective sensor infection. To this end, complementary fluorescent forced-intercalation (IAV...

10.1002/cbic.201700271 article EN ChemBioChem 2017-05-30

Corrected by: Cobalt-Catalyzed Cross-Coupling Reactions of Heterocyclic Chlorides with Arylmagnesium Halides and Polyfunctionalized Arylcopper Reagents Aryl Bromides, Chlorides, Fluorides TosylatesSynthesis 2006; 2006(24): 4270-4270DOI: 10.1055/s-2006-950377

10.1055/s-2006-950290 article EN Synthesis 2006-10-26

Correction to: Cobalt-Catalyzed Cross-Coupling Reactions of Heterocyclic Chlorides with Arylmagnesium Halides and Polyfunctionalized Arylcopper Reagents Aryl Bromides, Chlorides, Fluorides TosylatesSynthesis 2006; 2006(21): 3547-3574DOI: 10.1055/s-2006-950290

10.1055/s-2006-950377 article EN Synthesis 2006-12-11

ABSTRACT Orthohantaviruses, are emerging zoonotic pathogens causing life-threatening diseases in humans. The orthohantavirus genome consists of three RNA segment (vRNAs) negative polarity, which encapsidated by the viral nucleoprotein (N). To date, precise subcellular behavior vRNAs and N has not been fully elucidated. Here, we present a comprehensive analysis infections using Fluorescence situ Hybridization (FISH) multiple sequential FISH (Mu-Seq FISH), enables simultaneous detection RNAs,...

10.1101/2024.07.16.603662 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2024-07-16

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 200 leading journals. To access Abstract, please click on HTML or PDF.

10.1002/chin.200712092 article EN ChemInform 2007-03-01
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