Found 415 results
[ Author(Desc)] Title Type Year
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Vaníková, Z.; Hocek, M. Polymerase Synthesis of Photocaged DNA Resistant against Cleavage by Restriction Endonucleases. Angewandte Chemie International Edition 2014, 53 (26), 6734-6737 DOI: 10.1002/anie.201402370.
Veith, G. M.; Baggetto, L.; Adamczyk, L. A.; Guo, B.; Brown, S. S.; Sun, X. - G.; Albert, A. A.; Humble, J. R.; Barnes, C. E.; Bojdys, M. J.; et al. Electrochemical and Solid-State Lithiation of Graphitic C 3 N 4. Chemistry of Materials 2013, 25 (3), 503-508 DOI: 10.1021/cm303870x.
Vesely, J.; Ledvina, M.; Jindřich, J.; Šaman, D.; Trnka, T. Improved Synthesis of 1,2-trans-Acetates and 1,2-trans Ethyl 1-Thioglycosides Derived from 3,4,6-Tri-O-acetyl-2-deoxy-2-phthalimido-D-hexopyranosides. Collection of Czechoslovak Chemical Communications 2003, 68 (7), 1264-1274 DOI: 10.1135/cccc20031264.
Vesely, J.; Ledvina, M.; Jindrich, J.; Trnka, T.; Saman, D. 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.
Vesely, J.; Rios, R. Organocatalytic Enantioselective α-Alkylation of Aldehydes. ChemCatChem 2012, 4 (7), 942-953 DOI: 10.1002/cctc.201200072.
Vesely, J.; Rios, R. Enantioselective methodologies using N-carbamoyl-imines. Chem. Soc. Rev. 2014, 43 (2), 611-630 DOI: 10.1039/C3CS60321K.
Vlašaná, K.; Hrdina, R.; Valterová, I.; Kotora, M. 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.
Vrkoslav, V.; Jelinek, I.; Trojan, T.; Jindrich, J.; Dian, J. 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.
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