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Tomasz
Rowicki, Ph.D., Eng.
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tomek@ch.pw.edu.pl tel.:
(+48 22) 234 73 73 room 135
Wersja
polska
Research
topics
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Selected
publications:
T. Rowicki, I. D. Madura, P. H. Marek, K. Kopczyńska, E. Mironiuk-Puchalska, W. Sas "Synthesis,
structure of 7-oxa-1-aza-bicyclo[2.2.1]heptane derivative obtained from sugar nitrone and analysis of its conformational variety" J. Mol. Struct., 2019, 1183, 14-23
S. Molchanov, T. Rowicki,
A. Gryff-Keller, W. Koźmiński "Conformational Equilibrium of Cinchonidine in C6D12 Solution. Alternative NMR/DFT Approach" J. Phys. Chem. A, 2018, 122, 763-771
M. Malinowski, T. Rowicki,
P. Guzik, M. Wielechowska, W. Sas "Synthesis of carbohydrate mimetics by intramolecular 1,3-dipolar cycloaddition of N-(3-alkenyl)nitrones
derived from unprotected D-aldopentoses" Eur. J. Org. Chem., 2018, 763-771
T. Rowicki
"Iminosugars and related heterocycles with quaternary carbon adjacent to nitrogen: synthesis and biological properties" in Targets in Heterocyclic Systems, O.A. Attanasi,
P. Merino, D. Spinelli, Eds.; Italian Society of Chemistry, 2017, pp. 409-447
M. Malinowski, T. Rowicki,
P. Guzik, M. Wielechowska, A. Sobiepanek, W. Sas "Diversity-Oriented Synthesis and Biological Evaluation of Iminosugars from Unprotected 2-Deoxy-D-ribose" Eur.
J. Org. Chem., 2016, 3642-3649
M. Malinowski,
T. Rowicki, P. Guzik, M. Gryszel, S. Łapczyński, M. Wielechowska, K. Czerwińska, I. Madura, W. Sas "[1,4]-sigmatropic rearrangement of chiral nitrones and
their utilization in the synthesis of new iminosugars" Org. Biomol. Chem., 2016, 14, 470-482
T. Rowicki,
M. Malinowski, S. Łapczyński, M. Gryszel, K. Czerwińska, I. Madura, W. Sas "Epimerization of the alpha Stereocenter in D-Ribose-Derived Nitrones: Direct
Access to Variant Quinolizidines with D-Ribo and D-Arabino Configurations" Asian J. Org. Chem., 2015, 4, 733-736
T. Rowicki,
M. Malinowski, M. Gryszel, K. Czerwińska, I. Madura, E. Mironiuk-Puchalska, M. Koszytkowska-Stawińska, W. Sas "Unprotected Xylose-Derived Nitrone in
Stereodivergent Synthesis of 4-hydroxypiperidine Enantiomers: Weak Lewis Acid Induced Alteration of Stereochemistry in 1,3-Dipolar Cycloaddition" Eur.
J. Org. Chem., 2015, 1533-1540
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