1. T.Trnka, M.Černý, M.Buděšínský, J.Pacák: Syntheses with anhydrosugars XXV. Synthesis of 3-amino-3-deoxy-D-glucose (kanosamine) and its 1,6-anhydroderivative. Conformation of aminoderivatives of 1,6-anhydro-ß-D-hexopyranoses. Coll. Czech. Chem. Commun. 40, 3038-3045 (1975).
  2. T.Trnka, M.Černý: Syntheses with anhydrosugars X. Cleavage of oxirane ring in 1,6:3,4-dianhydro-ß-D-hexopyranoses with potassium hydroxide and sulfuric acid. Coll. Czech. Chem. Commun. 36, 2216-2225 (1971).
  3. .T.Trnka, M.Černý: Syntheses with anhydrosugars XIII. Preparation of deoxyderivatives of 1,6-anhydro-β-D-hexopyranoses by catalytic reduction of 1,6:2,3- and 1,6:3,4-dianhydro-ß-D-hexopyranoses. Coll. Czech. Chem. Commun. 37, 3632-3639 (1972).
  4. Zelenka, K., Trnka, T., Tišlerová, I., Král, V., Dukh, M., Drašar, P.: Synthesis of porphyrin receptors modified by glycosylated steroids, Collect.  Czech.  Chem, Commun.  69 (5): 1149-1160 (2004).

5.      Trtek, T., Černý, M., Buděšínský, M., Trnka, T. Císařová, I.: Synthesis of 1,6-anhydro-β-d-hexopyranoses fused to the piperidine ring. Collect.Czech. Chem. Commun. 70, 1429-1445 (2005).

  1. Dzoganova M, Cerny M, Budesinsky M, Dracinsky, M., Trnka, T.:  Epoxide migration and pseudo-epoxide migration of 1,6 : 2,3- and 1,6 : 3,4-dianhydro-beta-D-hexopyranoses. Synthesis of some deoxy halo derivatives of 1,6-anhydro-beta-D-hexopyranoses  Collect.  Czech.  Chem, Commun.  71, 1497-1515 (2006).
  2. Turský, M., Veselý, J.,  Tišlerová, I.,  Trnka, T.,  Ledvina, M.: Synthesis of a New Type of d-Mannosamine Glycosyl Donor and Acceptor and their Use for the Preparation of Oligosaccharides Consisting of d-Mannosamine Units Linked by α(1→4)-Glycosidic Bonds. Synthesis 2610-2616 (2008).
  3. Zahradnickova, H., Jegorov, A., Trnka, T., Zelenka, K.: Thiosugars - Derivatization agents for chiral resolution of homoleucines. J. Sep. Sci. 31,  133-136 (2008).
  4. A.Jegorov, J.Tříska,T.Trnka , M.Černý: Separation of a-aminoacids enantiomers by reversed-phase HPLC after derivatization with o-phtaldialdehyde and sodium salt of 1-thio-ß-D-glucose. J. Chromatogr. 434, 4l7-422 (1988).
  5. A.Jegorov, T.Trnka, J.Stuchlík: High Performance liquid chromatographic detection of enantiomeric amino alcohols after derivatization with o-phthaldialdehyde and various thiosugars. J.Chromatogr. 558, 311-317, (1991)

11.  Zelenka, K.,  Trnka, T.,  Tišlerová, I.,  Monti, D.,  Cinti, S.,  Naitana, M.L., Schiaffino, L., Venanzi, M.,  Laguzzi, G Luvidi, L.,  Mancini, G., Nováková, Z.,  Šimák, O., Sommer, Z.,  Drašar, P.  Spectroscopic, Morphological, and Mechanistic Investigation of the Solvent-Promoted Aggregation of Porphyrins Modified in meso-Positions by Glucosylated Steroids. Chem. Eur. J. 17, 13743 – 13753, (2011)

12.  Lettieri, R., Monti, D., Zelenka, K., Trnka, T., Drašar, P., Venazi, M. Glucysalated steroid-porphyrins as new tools  for nanotechnology applications. New J. Chem. DOI: 10.1039/c2nj20982a