Search results
- 1.0485398 - ÚOCHB 2018 CZ eng A - Abstract
Šimek, Michal - Jahn, Ullrich
Tandem Anionic oxy-Cope rearrangement/Radical reactions.
Liblice 2017. 52nd Advances in Organic, Bioorganic and Pharmaceutical Chemistry. Praha: Czech Chemical Society, 2017. s. 114.
[Liblice 2017. Advances in Organic, Bioorganic and Pharmaceutical Chemistry /52./. 03.11.2017-05.11.2017, Lázně Bělohrad]
R&D Projects: GA ČR(CZ) GA16-18513S
Institutional support: RVO:61388963
Keywords : AOC * single-electron oxidation
Subject RIV: CC - Organic Chemistry
Permanent Link: http://hdl.handle.net/11104/0280602 - 2.0485382 - ÚOCHB 2018 CZ eng A - Abstract
Provazníková, Adéla - Šimon, Petr - Šácha, Pavel - Konvalinka, Jan
His-tag Binding Ligand for iBodies: Tetrakis-nitrilotriacetic Acid.
Liblice 2017. 52nd Advances in Organic, Bioorganic and Pharmaceutical Chemistry. Praha: Czech Chemical Society, 2017. s. 111.
[Liblice 2017. Advances in Organic, Bioorganic and Pharmaceutical Chemistry /52./. 03.11.2017-05.11.2017, Lázně Bělohrad]
R&D Projects: GA ČR(CZ) GA16-02938S
Institutional support: RVO:61388963
Keywords : polyhistidine tag * iBodies * NTA
Subject RIV: CE - Biochemistry
Permanent Link: http://hdl.handle.net/11104/0280600 - 3.0485378 - ÚOCHB 2018 CZ eng A - Abstract
Tatar, Ameneh - Pramthaisong, Chiranan - Jahn, Ullrich
Photoredox-Catalysed C-H Amination Reactions with Nonafluorobutanesulfonyl Azide.
Liblice 2017. 52nd Advances in Organic, Bioorganic and Pharmaceutical Chemistry. Praha: Czech Chemical Society, 2017. s. 110.
[Liblice 2017. Advances in Organic, Bioorganic and Pharmaceutical Chemistry /52./. 03.11.2017-05.11.2017, Lázně Bělohrad]
R&D Projects: GA ČR(CZ) GA17-14510S
Institutional support: RVO:61388963
Keywords : photoredox catalysis * azides
Subject RIV: CC - Organic Chemistry
Permanent Link: http://hdl.handle.net/11104/0280589 - 4.0485373 - ÚOCHB 2018 CZ eng A - Abstract
Mašek, Tomáš - Jahn, Ullrich
Oxidative C-C Bond Cleavage of ketone enolates by nitrosation.
Liblice 2017. 52nd Advances in Organic, Bioorganic and Pharmaceutical Chemistry. Praha: Czech Chemical Society, 2017. s. 99.
[Liblice 2017. Advances in Organic, Bioorganic and Pharmaceutical Chemistry /52./. 03.11.2017-05.11.2017, Lázně Bělohrad]
R&D Projects: GA ČR GA13-40188S
Institutional support: RVO:61388963
Keywords : oxidative cleavage * ketones
Subject RIV: CC - Organic Chemistry
Permanent Link: http://hdl.handle.net/11104/0280582 - 5.0476672 - ÚOCHB 2018 CZ eng A - Abstract
Mašek, Tomáš - Presová, Gabriela - Jahn, Ullrich
Oxidative intermediate switching for the total synthesis of lignans.
Czech Chemical Society Symposium Series. Roč. 15, č. 1 (2017), s. 20-21. ISSN 2336-7202.
[Mezioborové setkání mladých biologů, biochemiků a chemiků /17./. 30.05.2017-01.06.2017, Milovy]
R&D Projects: GA ČR GA13-40188S
Institutional support: RVO:61388963
Keywords : lignans * total synthesis
Subject RIV: CC - Organic Chemistry
Permanent Link: http://hdl.handle.net/11104/0273129 - 6.0471208 - ÚOCHB 2017 CZ eng A - Abstract
Milisavljevič, Nemanja - Perlíková, Pavla - Hocek, Michal
Synthesis of base modified nucleoside triphosphates for the construction of modified RNAs.
Liblice 2016. 51st Advances in Organic, Bioorganic and Pharmaceutical Chemistry. Praha: Czech Chemical Society, 2016. s. 113.
[Liblice 2016. Advances in Organic, Bioorganic and Pharmaceutical Chemistry /51./. 11.11.2016-13.11.2016, Lázně Bělohrad]
R&D Projects: GA ČR GBP206/12/G151
Institutional support: RVO:61388963
Keywords : modified RNA * base modified triphosphates
Subject RIV: CC - Organic Chemistry
Permanent Link: http://hdl.handle.net/11104/0268787 - 7.0471204 - ÚOCHB 2017 CZ eng A - Abstract
Klívar, Jiří - Jančařík, Andrej - Bednárová, Lucie - Starý, Ivo - Stará, Irena G.
Pyridohelicenes via cyanodiynes.
Liblice 2016. 51st Advances in Organic, Bioorganic and Pharmaceutical Chemistry. Praha: Czech Chemical Society, 2016. s. 94.
[Liblice 2016. Advances in Organic, Bioorganic and Pharmaceutical Chemistry /51./. 11.11.2016-13.11.2016, Lázně Bělohrad]
R&D Projects: GA ČR(CZ) GA14-29667S
Institutional support: RVO:61388963
Keywords : pyridohelicenes * cyanodiynes * cycloisomerization
Subject RIV: CC - Organic Chemistry
Permanent Link: http://hdl.handle.net/11104/0268780 - 8.0471164 - ÚOCHB 2017 CZ eng A - Abstract
Holec, Jan - Rybáček, Jiří - Bednárová, Lucie - Stará, Irena G. - Starý, Ivo
Self-assembly of amphiphilic helicenes into thin films.
Liblice 2016. 51st Advances in Organic, Bioorganic and Pharmaceutical Chemistry. Praha: Czech Chemical Society, 2016. s. 79.
[Liblice 2016. Advances in Organic, Bioorganic and Pharmaceutical Chemistry /51./. 11.11.2016-13.11.2016, Lázně Bělohrad]
R&D Projects: GA ČR(CZ) GA16-08327S
Institutional support: RVO:61388963
Keywords : helicenes * dibenzo[6]helicene * monolayer formation
Subject RIV: CC - Organic Chemistry
Permanent Link: http://hdl.handle.net/11104/0268762 - 9.0471150 - ÚOCHB 2017 CZ eng A - Abstract
Downey, Alan Michael - Hocek, Michal
Protecting group-free glycosylation for the synthesis of nucleosides via an anhydrose intermediate.
Liblice 2016. 51st Advances in Organic, Bioorganic and Pharmaceutical Chemistry. Praha: Czech Chemical Society, 2016. s. 71.
[Liblice 2016. Advances in Organic, Bioorganic and Pharmaceutical Chemistry /51./. 11.11.2016-13.11.2016, Lázně Bělohrad]
R&D Projects: GA ČR GAP207/11/0344; GA ČR(CZ) GA16-00178S
Institutional support: RVO:61388963
Keywords : nucleoside synthesis * anhydrose * modified nucleosides
Subject RIV: CC - Organic Chemistry
Permanent Link: http://hdl.handle.net/11104/0268761 - 10.0471117 - ÚOCHB 2017 CZ eng A - Abstract
Houska, Václav - Stará, Irena G. - Starý, Ivo
Searching for a path towards helicene-based macrocycles.
Liblice 2016. 51st Advances in Organic, Bioorganic and Pharmaceutical Chemistry. Praha: Czech Chemical Society, 2016. s. 40.
[Liblice 2016. Advances in Organic, Bioorganic and Pharmaceutical Chemistry /51./. 11.11.2016-13.11.2016, Lázně Bělohrad]
R&D Projects: GA ČR(CZ) GA16-08294S
Institutional support: RVO:61388963
Keywords : helicene-based macrocycles * dibenzo[5]helicene
Subject RIV: CC - Organic Chemistry
Permanent Link: http://hdl.handle.net/11104/0268752