Publications
Found 384 results
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Enantioselective Allylation of Selected ortho-Substituted Benzaldehydes: A Comparative Study. European Journal of Organic Chemistry 2014, 2014 (32), 7245-7252 DOI: 10.1002/ejoc.201403034.
Enantioselective Allylation of tert-Butyldimethylsilyl-Protected Vanillin and Synthesis of a Lignan Derivative Isolated from Machilus wangchiana. European Journal of Organic Chemistry 2014, 2014 (34), 7556-7560 DOI: 10.1002/ejoc.201403094.
Enantioselective Allylation of tert-Butyldimethylsilyl-Protected Vanillin and Synthesis of a Lignan Derivative Isolated from Machilus wangchiana. European Journal of Organic Chemistry 2014, 2014 (34), 7556-7560 DOI: 10.1002/ejoc.201403094.
Enantioselective Allylation of Thiophene-2-carbaldehyde: Formal Total Synthesis of Duloxetine. Advanced Synthesis & Catalysis 2014, 356 (1), 199-204 DOI: 10.1002/adsc.201300849.
Examination of small molecule losses in 5-methylpyranopelargonidin MS/MS CID spectra by DFT calculations: MS/MS and DFT of 5-methylpyranopelargonidin. Journal of Mass Spectrometry 2014, 49 (12), 1314-1321 DOI: 10.1002/jms.3466.
The influence of the substituent position in monocarboxymethyl-γ-cyclodextrins on enantioselectivity in capillary electrophoresis. Journal of Separation Science 2014, 37 (19), 2779-2784 DOI: 10.1002/jssc.201400604.
Medicinal applications of perfluoroalkylated chain-containing compounds. Future Medicinal Chemistry 2014, 6 (10), 1201-1229 DOI: 10.4155/fmc.14.53.
Monensin inhibits canonical wnt signaling in human colorectal cancer cells and suppresses tumor growth in multiple intestinal neoplasia mice. Molecular cancer therapeutics 2014, 13 (4), 812-822 DOI: 10.1158/1535-7163.MCT-13-0625.
Monensin inhibits canonical wnt signaling in human colorectal cancer cells and suppresses tumor growth in multiple intestinal neoplasia mice. Molecular cancer therapeutics 2014, 13 (4), 812-822 DOI: 10.1158/1535-7163.MCT-13-0625.
Monensin inhibits canonical wnt signaling in human colorectal cancer cells and suppresses tumor growth in multiple intestinal neoplasia mice. Molecular cancer therapeutics 2014, 13 (4), 812-822 DOI: 10.1158/1535-7163.MCT-13-0625.
Organocatalytic enantioselective allylic alkylation of MBH carbonates with β-keto esters. Organic & Biomolecular Chemistry 2014, 12 (28), 5071 DOI: 10.1039/c4ob00682h.
Proton Affinities of Organocatalysts Derived from Pyridine N-oxide. Croatica Chemica Acta 2014, 87 (4), 349-356 DOI: 10.5562/cca2447.
Proton Affinities of Organocatalysts Derived from Pyridine N-oxide. Croatica Chemica Acta 2014, 87 (4), 349-356 DOI: 10.5562/cca2447.
Structural Basis for Inhibition of Mycobacterial and Human Adenosine Kinase by 7-Substituted 7-(Het)aryl-7-deazaadenine Ribonucleosides. Journal of Medicinal Chemistry 2014, 57 (20), 8268-8279 DOI: 10.1021/jm500497v.
Syntheses of a Flobufen Metabolite and Dapoxetine Based on Enantioselective Allylation of Aromatic Aldehydes: Syntheses of a Flobufen Metabolite and Dapoxetine. European Journal of Organic Chemistry 2014, 2014 (12), 2543-2548 DOI: 10.1002/ejoc.201301899.
Syntheses of a Flobufen Metabolite and Dapoxetine Based on Enantioselective Allylation of Aromatic Aldehydes: Syntheses of a Flobufen Metabolite and Dapoxetine. European Journal of Organic Chemistry 2014, 2014 (12), 2543-2548 DOI: 10.1002/ejoc.201301899.
Synthesis, Cytostatic, Antimicrobial, and Anti-HCV Activity of 6-Substituted 7-(Het)aryl-7-deazapurine Ribonucleosides. Journal of Medicinal Chemistry 2014, 57 (3), 1097-1110 DOI: 10.1021/jm4018948.
Synthesis, Cytostatic, Antimicrobial, and Anti-HCV Activity of 6-Substituted 7-(Het)aryl-7-deazapurine Ribonucleosides. Journal of Medicinal Chemistry 2014, 57 (3), 1097-1110 DOI: 10.1021/jm4018948.
Systematic exploration of a class of hydrophobic unnatural base pairs yields multiple new candidates for the expansion of the genetic alphabet. Nucleic Acids Research 2014, 42 (16), 10235-10244 DOI: 10.1093/nar/gku715.
Triazine-Based Graphitic Carbon Nitride: a Two-Dimensional Semiconductor. Angewandte Chemie 2014, 126 (29), 7580-7585 DOI: 10.1002/ange.201402191.
Triazine-Based Graphitic Carbon Nitride: a Two-Dimensional Semiconductor. Angewandte Chemie International Edition 2014, 53 (29), 7450-7455 DOI: 10.1002/anie.201402191.
Triazine-Based Graphitic Carbon Nitride: a Two-Dimensional Semiconductor. Angewandte Chemie International Edition 2014, 53 (29), 7450-7455 DOI: 10.1002/anie.201402191.
Triazine-Based Graphitic Carbon Nitride: a Two-Dimensional Semiconductor. Angewandte Chemie International Edition 2014, 53 (29), 7450-7455 DOI: 10.1002/anie.201402191.
Triazine-Based Graphitic Carbon Nitride: a Two-Dimensional Semiconductor. Angewandte Chemie 2014, 126 (29), 7580-7585 DOI: 10.1002/ange.201402191.
Triazine-Based Graphitic Carbon Nitride: a Two-Dimensional Semiconductor. Angewandte Chemie 2014, 126 (29), 7580-7585 DOI: 10.1002/ange.201402191.