Thomas Maier
University of Konstanz
9 Papers
113 Citations
Thomas Maier is an academic researcher from University of Konstanz. The author has contributed to research in topics: Nucleotide & Fluorescein. The author has an hindex of 5, co-authored 9 publications.
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Papers
Synthesis of d-ribo- and l-lyxo-phytosphingosine: Transformation into the corresponding lactosyl-ceramides
Richard R. Schmidt,Thomas Maier +1 more
TL;DR: In this paper, azido derivatives were transformed via regioselective mesylation, azide displacement, benzylidene cleavage, and azide reduction, into d - ribo -phytosphingosine and l - lyxo-phytophysine, respectively.
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Synthesis and Properties of New Fluorescein-Labeled Oligonucleotides
Thomas Maier,Wolfgang Pfleiderer +1 more
TL;DR: 2,4-Dinitroaniline is an efficient intramolecular fluorescence-quencher for fluorescein - labeled oligonucleotides and interacts with the heterocyclic bases on duplex formation, and fluorescescein shows strong fluorescence in a duplex form.
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A New Type of Fluorescence Labeling of Nucleosides, Nucleotides and Oligonucleotides
TL;DR: Fluorescein has been coupled to the amino groups of the common nucleo-sides via a carbamoyl spacer to form a new type of conjugates to be prepared with Npe and Npeoc protecting groups for application in oligonucleotide synthesis.
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Memory for Spatial and Temporal Order in Aphasics and Right Hemisphere Damaged Patients
TL;DR: Aphasics made significantly more errors than RHD and normals in both the spatial and the temporal task, while RHD were significantly impaired in comparison to the normal controls only in the spatial task.
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Synthesis of methyl 4-acetamido-2,4-dideoxy-d-glycero-d-galacto-octopyranoside, a decarboxyneuraminic acid analogue
Thomas Maier,Richard R. Schmidt +1 more
TL;DR: In this article, the Wittig reaction was used to transform 3,4-O-Isopropylidene-d -arabinose into (E/Z )-2,3, 4-trideoxy-6,7- O -isopropylene-d-carabinose, d - arabino -oct-3-enose propane-1,3-diyl acetal.
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