Publications

Found 22 results
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Jindrich, J.; Pitha, J.; Lindberg, B. Separation of cyclodextrins and their derivatives by thin-layer and preparative column chromatography. Carbohydrate Research 1995, 275 (1), 1-7.
Jindrich, J.; Cerny, M.; Trnka, T.; Budesinsky, M. Synhteses with Anhydro Sugars .39. The Synthesis of 4-O-Oligoethylene Glycol Derivatives of 1,6-Anhydro-beta-D-glycopyranos and Crown-ethers Formed by Their Intramolecular Cyclization. Collection of Czechoslovak Chemical Communications 1991, 56 (12), 2950-2963.
Reisinger, A.; Pecka, J.; Jindrich, J.; Miller, J. R.; Kirby, J. P.; Pospisil, L.; Michl, J. Synthesis and properties of thiol-terminated pyridinium wires. Abstracts of Papers of the American Chemical Society 2000, 220, 300-COLL.
Jindrich, J.; Harata, K.; Lindberg, B.; Pitha, J.; Seffers, P. Synthesis of 2(1),3(1)-O-(propane-1,2-diyl)- and 2(1),3(1)-O-(3-hydroxypropane-1,2-diyl)cyclomaltoheptaose. Carbohydrate Research 1997, 300 (4), 361-363.
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.
Jindrich, J.; Dvorakova, H.; Holy, A. Synthesis of Isomeric N-(3-Fluoro-2-hydroxypropyl) and N-(2-Fluoro-3-hydroxypropyl) Derivatives of Purine and Pyrimidine-bases. Collection of Czechoslovak Chemical Communications 1992, 57 (7), 1466-1482.
Jindrich, J.; Holy, A.; Dvorakova, H. Synthesis of N-(3-Fluoro-2-phophonomethoxypropyl) (FPMP) Derivatives of Heterocyclic Bases. Collection of Czechoslovak Chemical Communications 1993, 58 (7), 1645-1667.
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Dian, J.; Holec, T.; Jelinek, I.; Jindrich, J.; Valenta, J.; Pelant, I. Time evolution of photoluminescence response from porous silicon in hydrocarbon gas sensing. Physica Status Solidi A-Applied Research 2000, 182 (1), 485-488 DOI: 10.1002/1521-396X(200011)182:1<485::AID-PSSA485>3.0.CO;2-8.
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