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Thomas Michael Haas

Chemiker

Name	Thomas Michael Haas
Ort	Freiburg im Breisgau (Wirkungsort) Achern (Geburtsort) Deutschland
Akademischer Grad bzw. Titel	B.Sc.
Beruf	Chemiker (charakteristischer Beruf)
Weitere Angaben	Dissertation 2022, Albert-Ludwigs-Universität Freiburg im Breisgau, Fakultät für Chemie und Pharmazie
Datensatztyp	Person
GND-Nummer	1127883690
Datensatz-ID	1127883690
Beteiligt an alle anzeigen Bacterial pathogen infection triggers magic spot nucleotide signaling in Arabidopsis thaliana chloroplasts through specific RelA/SpoT homologues Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18 O‐Phosphoramidites Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18 O‐Phosphoramidites Photoaffinity capture compounds to profile the magic spot nucleotide interactomes Stable isotope phosphate labelling of diverse metabolites is enabled by a aamily of 18O-Phosphoramidites Stable isotope phosphate labelling of diverse metabolites is enabled by a family of 18o‐phosphoramidites The aryne phosphate reaction The aryne phosphate reaction Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18 O‐Phosphoramidites Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18 O‐Phosphoramidites ** The Aryne phosphate reaction Towards new tools in chemical biology - investigations on phosphate chemistry of magic spot nucleotides and aryne intermediates Analysis of inositol phosphate metabolism by capillary electrophoresis electrospray ionization mass spectrometry Four phosphates at one blow: access to pentaphosphorylated magic spot nucleotides and their analysis by capillary electrophoresis Thiocoumarin caged nucleotides: synthetic access and their photophysical properties Direct conjugate alkylation of α,β-unsaturated carbonyls by TiIII-catalysed reductive umpolung of simple activated alkenes

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Bacterial pathogen infection triggers magic spot nucleotide signaling in Arabidopsis thaliana chloroplasts through specific RelA/SpoT homologues

Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18 O‐Phosphoramidites

Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18 O‐Phosphoramidites

Photoaffinity capture compounds to profile the magic spot nucleotide interactomes**

Stable isotope phosphate labelling of diverse metabolites is enabled by a aamily of 18O-Phosphoramidites

Stable isotope phosphate labelling of diverse metabolites is enabled by a family of 18o‐phosphoramidites**

The aryne phosphate reaction

The aryne phosphate reaction**

Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18 O‐Phosphoramidites **

Stable Isotope Phosphate Labelling of Diverse Metabolites is Enabled by a Family of 18 O‐Phosphoramidites **

The Aryne phosphate reaction

Towards new tools in chemical biology - investigations on phosphate chemistry of magic spot nucleotides and aryne intermediates

Analysis of inositol phosphate metabolism by capillary electrophoresis electrospray ionization mass spectrometry

Four phosphates at one blow: access to pentaphosphorylated magic spot nucleotides and their analysis by capillary electrophoresis

Thiocoumarin caged nucleotides: synthetic access and their photophysical properties

Direct conjugate alkylation of α,β-unsaturated carbonyls by TiIII-catalysed reductive umpolung of simple activated alkenes