Publications
Found 60 results
[ Author] Title Type Year Filters: First Letter Of Last Name is K [Clear All Filters]
Synthesis of nucleosides and dNTPs bearing oligopyridine ligands linked through an octadiyne tether, their incorporation into DNA and complexation with transition metal cations. Org. Biomol. Chem. 2013, 11 (1), 78-89 DOI: 10.1039/C2OB26881G.
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.
Synthesis of selectively 4-substituted 9,9 '-spirobifluorenes and modulation of their photophysical properties. Organic & Biomolecular Chemistry 2017, 15 (33), 6913-6920 DOI: 10.1039/c7ob01319a.
Direct regioselective C-H borylation of [5]helicene. Rsc Advances 2018, 8 (1), 580-583 DOI: 10.1039/c7ra13021j.
Enantioselective epoxide ring opening catalyzed by bis(tetrahydroisoquinoline) N,N′-dioxides. Collection of Czechoslovak Chemical Communications 2011, 76 (5), 415-422 DOI: 10.1135/cccc2011024.
Lewis Base Catalyzed Enantioselective Allylation of α,β-Unsaturated Aldehydes. Chemistry - A European Journal 2010, 16 (31), 9442-9445 DOI: 10.1002/chem.201001523.
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.
Simple and Fast Synthesis of New Axially Chiral Bipyridine N,N′ -Dioxides for Highly Enantioselective Allylation of Aldehydes. Advanced Synthesis & Catalysis 2009, 351 (9), 1279-1283 DOI: 10.1002/adsc.200900224.
ChemInform Abstract: Enantioselective Epoxide Ring Opening Catalyzed by Bis(tetrahydroisoquinoline) N,N′-Dioxides. ChemInform 2011, 42 (35), no-no DOI: 10.1002/chin.201135031.
Nucleophile-assisted cyclization of beta-propargylamino acrylic compounds catalyzed by gold(I): a rapid construction of multisubstituted tetrahydropyridines and their fused derivatives. Organic Chemistry Frontiers 2020, 7 (21), 3356-3367 DOI: 10.1039/d0qo00653j.