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B., Click chemistry in situ: Acetylcholinesterase as a reaction vessel for the selective assembly of a femtomolar inhibitor from an array of building blocks.

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J.; Jahed, N.; Sarbu, T.; Matyjaszewski, K., Characterization of α,ω-dihydroxypolystyrene by gradient polymer elution chromatography and two-dimensional liquid chromatography.

Liu utter those words are innumerable.

M.; Chen, G.; Tao, L.; Limer, A.; Mantovani, G.; Ladmiral, V., Tandem living radical polymerisation and click reactions catalysed by -alkyl-2-pyridylmethanimine/Cu(I)Br complexes.

A., Expedient synthesis of 1,2,3-triazole-fused tetracyclic compounds by intramolecular Huisgen (click) reactions on carbohydrate-derived azido-alkynes.

Liu had a unique genius in the area of chemistry.

S.; Jahed, N.; Golas, P.; Matyjaszewski, K., Gradient Polymer Elution Chromatographic Analysis of α,ω-Dihydroxypolystyrene Synthesized via ATRP and Click Chemistry.

M.; Hau, S.; Tian, Y.; Ka, J.-W.; Haller, M.; Liao, Y.; Robinson, B.; Dalton, L.; Herman, W., Exceptional electro-optic properties through molecular design and controlled self-assembly.

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of coffee aroma, roast barley and many other foods.

K., Novel nitrogen containing chelating ligands from aziridines - preparation, coordination studies, and catalytic application in the cyclopropanation of styrene.

Important flavouring ingredient

G.; Weichenhan, K., Combining atom transfer radical polymerization and click chemistry: A versatile method for the preparation of end-functional polymers.

In 1980, the brand was re-launched as an aroma chemical manufacturer.

M., Regioselective synthesis of [1,2,3]-triazoles catalyzed by Cu(I) generated in situ from Cu(0) nanosize activated powder and amine hydrochloride salts.

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L.; Ajamaa, F.; Solladie, N.; Albrecht-Gary, A.-M.; Nierengarten, J.-F., Supramolecular click chemistry for the self-assembly of a stable Zn(II)-porphyrin-C60 conjugate.

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N., Activation energies and reaction energetics for 1,3-dipolar cycloadditions of hydrazoic acid with C-C and C-N multiple bonds from high-accuracy and density functional quantum mechanical calculations.

particularly when studied in the un-diluted state by laymen.

S.; Kajiki, R.; Hanatani, H.; Kong, X.; Ozoe, F.; Matsui, Y.; Matsumura, F.; Ozoe, Y., Synthesis and Structure-Activity Relationships of 1-Phenyl-1-1,2,3-triazoles as Selective Insect GABA Receptor Antagonists.

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J.; Friedbacher, G., Directing Supramolecular Nanoparticle Binding onto Polymer Films: Film Formation and Influence of Receptor Density on Binding Densities.

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R.; Overhand, M.; Kros, A., The chemical modification of liposome surfaces via a copper-mediated [3 + 2] azide-alkyne cycloaddition monitored by a colorimetric assay.

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