Publications
Found 129 results
Author Title Type [ Year
Filters: First Letter Of Last Name is V [Clear All Filters]
Highly enantioselective organocatalytic cascade reaction for the synthesis of piperidines and oxazolidines. Tetrahedron 2011, 67 (46), 8942-8950 DOI: 10.1016/j.tet.2011.08.079.
Highly enantioselective organocatalytic cascade reaction for the synthesis of piperidines and oxazolidines. Tetrahedron 2011, 67 (46), 8942-8950 DOI: 10.1016/j.tet.2011.08.079.
Synthesis and biological activity of desmethoxy analogues of coruscanone A. Bioorganic & Medicinal Chemistry Letters 2011, 21 (20), 6062-6066 DOI: 10.1016/j.bmcl.2011.08.059.
[2+2+2]-Cocyclotrimerization of 6-Alkynyl-7-benzylpurines with α,ω-Diynes. HETEROCYCLES 2010, 82 (1), 895 DOI: 10.3987/COM-10-S(E)56.
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 Aldehydes Catalyzed by Diastereoisomeric Bis(tetrahydroisoquinoline) N,N′-Dioxides. European Journal of Organic Chemistry 2010, 2010 (36), 7040-7044 DOI: 10.1002/ejoc.201001219.
Highly Enantioselective Addition of 1-Fluoro-1-nitro(phenylsulfonyl)methane to α,β-Unsaturated Aldehydes. European Journal of Organic Chemistry 2010, 2010 (28), 5464-5470 DOI: 10.1002/ejoc.201000851.
Lewis Base Catalyzed Enantioselective Allylation of α,β-Unsaturated Aldehydes. Chemistry - A European Journal 2010, 16 (31), 9442-9445 DOI: 10.1002/chem.201001523.
Highly Enantioselective Aza-Baylis–Hillman-Type Reaction of α,β-Unsaturated Aldehydes with In Situ Generated N -Boc- and N -Cbz-Imines. European Journal of Organic Chemistry 2009, 2009 (36), 6277-6280 DOI: 10.1002/ejoc.200900969.
Highly enantioselective fluoromalonate addition to α,β-unsaturated aldehydes. Tetrahedron Letters 2009, 50 (35), 5021-5024 DOI: 10.1016/j.tetlet.2009.06.092.
Highly enantioselective organocatalytic synthesis of piperidines. Formal synthesis of (−)-Paroxetine. Tetrahedron Letters 2009, 50 (17), 1943-1946 DOI: 10.1016/j.tetlet.2009.02.049.
Highly enantioselective organocatalytic synthesis of piperidines. Formal synthesis of (−)-Paroxetine. Tetrahedron Letters 2009, 50 (17), 1943-1946 DOI: 10.1016/j.tetlet.2009.02.049.
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.
Catalytic Asymmetric Allylation of Aliphatic Aldehydes by Chiral Bipyridine N,N '-Dioxides. Synlett 2008, 2008 (20), 3141-3144 DOI: 10.1055/s-0028-1087412.
Extension of the Library of Biologically Active γ-Alkylidene Butenolides. Synthesis 2008, 2008 (21), 3465-3472 DOI: 10.1055/s-0028-1083181.
New pathway to C-2-Symmetric atropoisomeric bipyridine N,N '-Dioxides and solvent effect in enantioselective allylation of aldehydes. Advanced Synthesis & Catalysis 2008, 350 (10), 1449-1456 DOI: 10.1002/adsc.200800141.
Permethylated 6(I)-alkenoylamino-6(I)-deoxy beta-cyclodextrin derivatives as modifiers of photoluminescence sensor response of porous silicon. Journal of Inclusion Phenomena and Macrocyclic Chemistry 2007, 57 (1-4), 343-348 DOI: 10.1007/s10847-006-9260-5.
Porous silicon with beta-cyclodextrin modified surface for photoluminescence sensing of organic molecules in gas and liquid phase. Physica E: Low-dimensional Systems & Nanostructures 2007, 38 (1-2), 200-204 DOI: 10.1016/j.physe.2006.12.052.
A Simple Approach to Unsymmetric Atropoisomeric BipyridineN,N′-Dioxides and Their Application in Enantioselective Allylation of Aldehydes. Advanced Synthesis & Catalysis 2007, 349 (6), 822-826 DOI: 10.1002/adsc.200600400.
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.
Nanostructured porous silicon - Optical properties, surface modification and sensor applications. Chimia 2005, 59 (5), 222-225.
Nonaqueous capillary electrophoretic assays of p-phenylene-bis-4,4'-(1-aryl-2,6-diphenylpyridinium) molecular wires. Electrophoresis 2005, 26 (23), 4465-4467 DOI: 10.1002/elps.200500414.
Oligomers of “Extended Viologen”, p-Phenylene-bis-4,4‘-(1-aryl-2,6-diphenylpyridinium), as Candidates for Electron-Dopable Molecular Wires. The Journal of Organic Chemistry 2005, 70 (2), 405-412 DOI: 10.1021/jo049142s.
Mechanisms of photoluminescence sensor response of porous silicon for organic species in gas and liquid phases. Sensors and Actuators, B: Chemical 2004, 100 (1-2), 246-249 DOI: 10.1016/j.snb.2003.12.040.
Synthesis of 2-amino-2-deoxy-beta-D-galactopyranosyl(1 -> 4)-2-amino-2-deoxy-beta-D-galactopyranosides: Using various 2-deoxy-2-phthalimido-D-galactopyranosyl donors and acceptors. Collection of Czechoslovak Chemical Communications 2004, 69 (10), 1914-1938 DOI: 10.1135/cccc20041914.