Publications
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A [2+2+2]-Cyclotrimerization Approach to Selectively Substituted Fluorenes and Fluorenols, and Their Conversion to 9,9′-Spirobifluorenes. Chemistry - A European Journal 2015, 21 (39), 13577-13582 DOI: 10.1002/chem.201502370.
A [2+2+2]-Cyclotrimerization Approach to Selectively Substituted Fluorenes and Fluorenols, and Their Conversion to 9,9′-Spirobifluorenes. Chemistry - A European Journal 2015, 21 (39), 13577-13582 DOI: 10.1002/chem.201502370.
Alkynylation of heterocyclic compounds using hypervalent iodine reagent. Org. Biomol. Chem. 2015, 13 (10), 2884-2889 DOI: 10.1039/C4OB02625J.
Cross-metathesis reaction of α- and β-vinyl C -glycosides with alkenes. Beilstein Journal of Organic Chemistry 2015, 11, 1392-1397 DOI: 10.3762/bjoc.11.150.
Enantioselective Allylation of (2E,4E)-2,4-Dimethylhexadienal: Synthesis of (5R,6S)-(+)-Pteroenone. Chemistry - A European Journal 2015, 21 (20), 7408-7412 DOI: 10.1002/chem.201500050.
Enantioselective Allylation of (2E,4E)-2,4-Dimethylhexadienal: Synthesis of (5R,6S)-(+)-Pteroenone. Chemistry - A European Journal 2015, 21 (20), 7408-7412 DOI: 10.1002/chem.201500050.
Modification of Pyrrolo[2,3-d]pyrimidines by C-H Borylation Followed by Cross-Coupling or Other Transformations: Synthesis of 6,8-Disubstituted 7-Deazapurine Bases. European Journal of Organic Chemistry 2015, 2015 (36), 7943-7961 DOI: 10.1002/ejoc.201501177.
Reaction of Bicyclic Zirconacyclopentenes with Aldehydes and a Potential Pathway to Condensed 5-7-6(Ar) Ring Systems: Reaction of Bicyclic Zirconacyclopentenes with Aldehydes. European Journal of Organic Chemistry 2015, 2015 (13), 2868-2878 DOI: 10.1002/ejoc.201500248.
Synthesis and cytostatic activity of 7-arylsulfanyl-7-deazapurine bases and ribonucleosides. Med. Chem. Commun. 2015, 6 (4), 576-580 DOI: 10.1039/C4MD00492B.
Synthesis of Benzene and Pyridine 2-C-Methyl-C-ribonucleosides and -nucleotides. European Journal of Organic Chemistry 2015, 2015 (36), 7962-7983 DOI: 10.1002/ejoc.201501219.
[2+2+2]-Cyclotrimerization of 1-Cyclopropyl-1,6-diynes with Alkynes: Formation of Cyclopropylarenes. Advanced Synthesis & Catalysis 2016, 358 (2), 254-267 DOI: 10.1002/adsc.201500851.
5-Substituted Pyrimidine and 7-Substituted 7-Deazapurine dNTPs as Substrates for DNA Polymerases in Competitive Primer Extension in the Presence of Natural dNTPs. ACS Chemical Biology 2016, 11 (11), 3165-3171 DOI: 10.1021/acschembio.6b00714.
Bisallylation of Zirconacyclopentenes and Ring-Closing Metathesis: A Route to Eight-Membered-Ring Compounds. Synlett 2016, 27 (03), 432-436 DOI: 10.1055/s-0035-1560587.
Chromatographic Characterization of a New Cationic β-CD Based Stationary Phase Prepared by Dynamic Coating. Chromatographia 2016, 79 (9-10), 529-536 DOI: 10.1007/s10337-016-3050-z.
Chromatographic Characterization of a New Cationic β-CD Based Stationary Phase Prepared by Dynamic Coating. Chromatographia 2016, 79 (9-10), 529-536 DOI: 10.1007/s10337-016-3050-z.
C–H Phosphonation of Pyrrolopyrimidines: Synthesis of Substituted 7- and 9-Deazapurine-8-phosphonate Derivatives. The Journal of Organic Chemistry 2016, 81 (19), 9507-9514 DOI: 10.1021/acs.joc.6b01970.
Enantioselective Allylation of β-Haloacrylaldehydes: Formal Total Syntheses of Pteroenone and Antillatoxin. European Journal of Organic Chemistry 2016, 2016 (12), 2110-2114 DOI: 10.1002/ejoc.201600286.
Enantioselective Allylation of β-Haloacrylaldehydes: Formal Total Syntheses of Pteroenone and Antillatoxin. European Journal of Organic Chemistry 2016, 2016 (12), 2110-2114 DOI: 10.1002/ejoc.201600286.
Enantioselective Synthesis of the Unsaturated Fragment of Callyspongiolide. Organic Letters 2016, 18 (21), 5656-5659 DOI: 10.1021/acs.orglett.6b02897.
Enantioselective Synthesis of the Unsaturated Fragment of Callyspongiolide. Organic Letters 2016, 18 (21), 5656-5659 DOI: 10.1021/acs.orglett.6b02897.
Flexible double-headed cytosine-linked 2′-deoxycytidine nucleotides. Synthesis, polymerase incorporation to DNA and interaction with DNA methyltransferases. Bioorganic & Medicinal Chemistry 2016, 24 (6), 1268-1276 DOI: 10.1016/j.bmc.2016.01.057.
Influence of major-groove chemical modifications of DNA on transcription by bacterial RNA polymerases. Nucleic Acids Research 2016, 44 (7), 3000-3012 DOI: 10.1093/nar/gkw171.
Influence of substituent position and cavity size of the regioisomers of monocarboxymethyl-α-, β-, and γ-cyclodextrins on the apparent stability constants of their complexes with both enantiomers of Tröger's base. Journal of Separation Science 2016, 39 (5), 980-985 DOI: 10.1002/jssc.201500845.
Kinetic, thermodynamic and structural analysis of tamiphosphor binding to neuraminidase of H1N1 (2009) pandemic influenza. European Journal of Medicinal Chemistry 2016, 121, 100-109 DOI: 10.1016/j.ejmech.2016.05.016.
Kinetic, thermodynamic and structural analysis of tamiphosphor binding to neuraminidase of H1N1 (2009) pandemic influenza. European Journal of Medicinal Chemistry 2016, 121, 100-109 DOI: 10.1016/j.ejmech.2016.05.016.