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.
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.
7-Aryl-7-deazaadenine 2′-Deoxyribonucleoside Triphosphates (dNTPs): Better Substrates for DNA Polymerases than dATP in Competitive Incorporations. Angewandte Chemie International Edition 2014, 53 (29), 7552-7555 DOI: 10.1002/anie.201404742.
Alpha (α-) and beta (β-carboranyl-C-deoxyribosides: Syntheses, structures and biological evaluation. European Journal of Medicinal Chemistry 2014, 83, 389-397 DOI: 10.1016/j.ejmech.2014.06.005.
C-H Trifluoromethylations of 1,3-Dimethyluracil and Reactivity of the Products in C-H Arylations. HETEROCYCLES 2014, 89 (5), 1159 DOI: 10.3987/COM-14-12958.
Chemoselective Synthesis of 4,5-Diarylpyrrolo[2,3-d]pyrimidines (6,7-Diaryl-7-deazapurines) by Consecutive Suzuki and Liebeskind-Srogl Cross-Couplings. European Journal of Organic Chemistry 2014, 2014 (32), 7203-7210 DOI: 10.1002/ejoc.201402882.
Chemoselective Synthesis of 4,5-Diarylpyrrolo[2,3-d]pyrimidines (6,7-Diaryl-7-deazapurines) by Consecutive Suzuki and Liebeskind-Srogl Cross-Couplings. European Journal of Organic Chemistry 2014, 2014 (32), 7203-7210 DOI: 10.1002/ejoc.201402882.
Chemoselective Synthesis of 4,5-Diarylpyrrolo[2,3-d]pyrimidines (6,7-Diaryl-7-deazapurines) by Consecutive Suzuki and Liebeskind-Srogl Cross-Couplings. European Journal of Organic Chemistry 2014, 2014 (32), 7203-7210 DOI: 10.1002/ejoc.201402882.
Cross-Coupling Reaction of Saccharide-Based Alkenyl Boronic Acids with Aryl Halides: The Synthesis of Bergenin. Chemistry - A European Journal 2014, 20 (15), 4414-4419 DOI: 10.1002/chem.201304304.
Cycloaddition Reactions of Deoxyribosylpropynoates. Synthetic Communications 2014, 44 (9), 1232-1239 DOI: 10.1080/00397911.2013.848896.
Cycloaddition Reactions of Deoxyribosylpropynoates. Synthetic Communications 2014, 44 (9), 1232-1239 DOI: 10.1080/00397911.2013.848896.
Direct C-H amination and C-H chloroamination of 7-deazapurines. RSC Adv. 2014 DOI: 10.1039/C4RA13143F.
Direct C-H amination and C-H chloroamination of 7-deazapurines. RSC Adv. 2014 DOI: 10.1039/C4RA13143F.
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 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.