Review of iron-free Fenton-like systems for activating H2O2 in advanced oxidation processes

Functional π-Gelators and Their Applications

Publisher Summary This chapter provides an overview of the 13 Carbon-nuclear magnetic resonance ( 13 C-NMR) spectroscopy of monosaccharides. The 13 C-NMR spectroscopy has become increasingly important as a tool for the characterization and structural elucidation of sugars and their derivatives. Although 13 C-NMR is closely related to 1 H-NMR spectroscopy, especially when both types of spectra are recorded with Fourier-transform instruments, the two techniques are sufficiently different to be valuable complements to each other. In many cases, in particular when dealing with complex molecules such as polysaccharides, the amount of information obtainable from 1 H-NMR spectra is limited as compared to that revealed by 13 C- NMR spectra. This chapter provides an almost complete collection of 13 C- NMR chemical shifts of monosaccharides, their methyl glycosides, and acetates, along with the examples of shift data for as many different types of monosaccharide derivative as possible. It also provides details on sampling techniques and assignment techniques, and discusses the identity of monosaccharides, their structure determination, and conformational analysis .

Carbon-13 Nuclear Magnetic Resonance Spectroscopy of Monosaccharides

10. Patented Literature 2616 10.1. Esterification 2616 10.2. Ether Formation 2619 10.2.1. Etherification without Cyclization 2619 10.2.2. Etherification with Cyclization 2624 10.3. N-Alkylation 2625 10.4. Other Reactions 2627 11. Summary and Outlook 2628 12. Note Added in Proof 2628 13. Abbreviations Used in This Review 2629 14. Acknowledgments 2629 15. Supporting Information Available 2630 16. References 2630

Mitsunobu and Related Reactions: Advances and Applications

Tandem Reaction Sequences under Hydroformylation Conditions: New Synthetic Applications of Transition Metal Catalysis.

Syntheses with anhydro sugars. X. Cleavage of oxiran ring in 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with potassium hydroxide and sulfuric acid

Decolorization of synthetic dyes using a copper complex with glucaric acid.

Separation of α-amino acid enantiomers by reversed phase high-performance liquid chromatography after derivatization with o-phthaldialdehyde and a sodium salt of 1-thio-β-d-glucose

Copper–ligand complex for the decolorization of synthetic dyes

The 1 H NMR spectra and the conformation of 1,6-anhydro-β-D-hexopyranoses and their triacetates

Tomáš Trnka

Papers

Syntheses with anhydro sugars. X. Cleavage of oxiran ring in 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses with potassium hydroxide and sulfuric acid

Decolorization of synthetic dyes using a copper complex with glucaric acid.

Separation of α-amino acid enantiomers by reversed phase high-performance liquid chromatography after derivatization with o-phthaldialdehyde and a sodium salt of 1-thio-β-d-glucose

Copper–ligand complex for the decolorization of synthetic dyes

The 1 H NMR spectra and the conformation of 1,6-anhydro-β-D-hexopyranoses and their triacetates