Publications
Found 301 results
Author Title [ Type] Year Filters: First Letter Of Last Name is K [Clear All Filters]
Cross-Cyclotrimerization with Two Nitriles as a Synthetic Pathway to Unsymmetrically 3,3’-Disubstituted bis(Tetrahydroisoquinolines). Molecules 2009, 14 (8), 2918-2926 DOI: 10.3390/molecules14082918.
Cross-metathesis of allylcarboranes with O-allylcyclodextrins. Beilstein Journal of Organic Chemistry 2010, 6, 1099-1105 DOI: 10.3762/bjoc.6.126.
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.
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.
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.
Development of a simple high-throughput assay for directed evolution of enantioselective sulfoxide reductases. Chemical Communications 2020, 56 (40), 5386-5388 DOI: 10.1039/d0cc01660h.
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.
Direct C–H sulfenylation of purines and deazapurines. Organic & Biomolecular Chemistry 2013, 11 (31), 5189 DOI: 10.1039/c3ob40881g.
Direct regioselective C-H borylation of [5]helicene. Rsc Advances 2018, 8 (1), 580-583 DOI: 10.1039/c7ra13021j.
Discovery of Modified Amidate (ProTide) Prodrugs of Tenofovir with Enhanced Antiviral Properties. Journal of Medicinal Chemistry 2021, 64 (22), 16425-16449.
Discovery of Modified Amidate (ProTide) Prodrugs of Tenofovir with Enhanced Antiviral Properties. Journal of Medicinal Chemistry 2021, 64 (22), 16425-16449.
(E)-7-Ethylidene-lithocholic Acid (7-ELCA) Is a Potent Dual Farnesoid X Receptor (FXR) Antagonist and GPBAR1 Agonist Inhibiting FXR-Induced Gene Expression in Hepatocytes and Stimulating Glucagon-like Peptide-1 Secretion From Enteroendocrine Cells. Frontiers in Pharmacology 2021, 12 (August), nestránkováno.
(E)-7-Ethylidene-lithocholic Acid (7-ELCA) Is a Potent Dual Farnesoid X Receptor (FXR) Antagonist and GPBAR1 Agonist Inhibiting FXR-Induced Gene Expression in Hepatocytes and Stimulating Glucagon-like Peptide-1 Secretion From Enteroendocrine Cells. Frontiers in Pharmacology 2021, 12 (August), nestránkováno.
(E)-7-Ethylidene-lithocholic Acid (7-ELCA) Is a Potent Dual Farnesoid X Receptor (FXR) Antagonist and GPBAR1 Agonist Inhibiting FXR-Induced Gene Expression in Hepatocytes and Stimulating Glucagon-like Peptide-1 Secretion From Enteroendocrine Cells. Frontiers in Pharmacology 2021, 12 (August), nestránkováno.
(E)-7-Ethylidene-lithocholic Acid (7-ELCA) Is a Potent Dual Farnesoid X Receptor (FXR) Antagonist and GPBAR1 Agonist Inhibiting FXR-Induced Gene Expression in Hepatocytes and Stimulating Glucagon-like Peptide-1 Secretion From Enteroendocrine Cells. Frontiers in Pharmacology 2021, 12 (August), nestránkováno.
An easy route to atropoisomeric bipyridine N,N′-dioxides and allylation of aldehydes. Tetrahedron: Asymmetry 2006, 17 (22), 3185-3191 DOI: 10.1016/j.tetasy.2006.11.025.
An easy route to atropoisomeric bipyridine N,N′-dioxides and allylation of aldehydes. Tetrahedron: Asymmetry 2006, 17 (22), 3185-3191 DOI: 10.1016/j.tetasy.2006.11.025.
Efficacy of the acyclic nucleoside phosphonates (S)-9-(3-fluoro-2-phosphonylmethoxypropyl)adenine (FPMPA) and 9-(2-phosphonylmethoxyethyl)adenine (PMEA) against feline immunodeficiency virus. Journal of Acquired Immune Deficiency Syndromes and Human Retrovirology 1998, 17 (2), 120-128.
Efficacy of the acyclic nucleoside phosphonates (S)-9-(3-fluoro-2-phosphonylmethoxypropyl)adenine (FPMPA) and 9-(2-phosphonylmethoxyethyl)adenine (PMEA) against feline immunodeficiency virus. Journal of Acquired Immune Deficiency Syndromes and Human Retrovirology 1998, 17 (2), 120-128.
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.
Enantioselective Allylation of Aldehydes Catalyzed by Diastereoisomeric Bis(tetrahydroisoquinoline) N,N′-Dioxides. European Journal of Organic Chemistry 2010, 2010 (36), 7040-7044 DOI: 10.1002/ejoc.201001219.
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.