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Jan Choutka

Showing results (1-10 of 13) with videos related to

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ACS Omega|August 29, 2019
MOP and EE Protecting Groups in Synthesis of α- or β-Naphthyl-<i>C</i>-Glycosides from GlycalsJan Choutka, Radek Pohl, Kamil Parkan
Nature Medicine|May 18, 2022
Unexplained post-acute infection syndromesJan Choutka, Viraj Jansari, Mady Hornig, et al.
Carbohydrate Research|January 3, 2024
On the origin of the electronic and magnetic circular dichroism of naphthyl C-glycosides: Anomeric configurationJan Choutka, Kamil Parkan, Radek Pohl, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|March 25, 2015
Modular Stereoselective Synthesis of (1→2)-C-Glycosides based on the sp(2) -sp(3) Suzuki-Miyaura ReactionBeata Oroszova, Jan Choutka, Radek Pohl, et al.
Nature Medicine|July 21, 2022
Author Correction: Unexplained post-acute infection syndromesJan Choutka, Viraj Jansari, Mady Hornig, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|May 28, 2021
Facile Approach to C-Glucosides by Using a Protecting-Group-Free Hiyama Cross-Coupling Reaction: High-Yielding Dapagliflozin SynthesisKarolína Vaňková, Michal Rahm, Jan Choutka, et al.
Carbohydrate Research|August 23, 2020
Straightforward synthesis of protected 2-hydroxyglycals by chlorination-dehydrochlorination of carbohydrate hemiacetalsJan Choutka, Michal Kratochvíl, Jakub Zýka, et al.
Journal of Chemical Information and Modeling|January 4, 2025
End-Point Affinity Estimation of Galectin Ligands by Classical and Semiempirical Quantum Mechanical PotentialsJan Choutka, Jakub Kaminský, Ercheng Wang, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|June 28, 2021
Facile Approach to C-Glucosides by Using a Protecting-Group-Free Hiyama Cross-Coupling Reaction: High-Yielding Dapagliflozin SynthesisKarolína Vaňková, Michal Rahm, Jan Choutka, et al.
Organic & Biomolecular Chemistry|July 21, 2022
Silicon-bridged (1→1)-disaccharides: an umpoled glycomimetic scaffoldJan Choutka, Michal Kratochvíl, Ivana Císařová, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
ACS Omega|August 29, 2019
MOP and EE Protecting Groups in Synthesis of α- or β-Naphthyl-<i>C</i>-Glycosides from GlycalsJan Choutka, Radek Pohl, Kamil Parkan
Nature Medicine|May 18, 2022
Unexplained post-acute infection syndromesJan Choutka, Viraj Jansari, Mady Hornig, et al.
Carbohydrate Research|January 3, 2024
On the origin of the electronic and magnetic circular dichroism of naphthyl C-glycosides: Anomeric configurationJan Choutka, Kamil Parkan, Radek Pohl, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|March 25, 2015
Modular Stereoselective Synthesis of (1→2)-C-Glycosides based on the sp(2) -sp(3) Suzuki-Miyaura ReactionBeata Oroszova, Jan Choutka, Radek Pohl, et al.
Nature Medicine|July 21, 2022
Author Correction: Unexplained post-acute infection syndromesJan Choutka, Viraj Jansari, Mady Hornig, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|May 28, 2021
Facile Approach to C-Glucosides by Using a Protecting-Group-Free Hiyama Cross-Coupling Reaction: High-Yielding Dapagliflozin SynthesisKarolína Vaňková, Michal Rahm, Jan Choutka, et al.
Carbohydrate Research|August 23, 2020
Straightforward synthesis of protected 2-hydroxyglycals by chlorination-dehydrochlorination of carbohydrate hemiacetalsJan Choutka, Michal Kratochvíl, Jakub Zýka, et al.
Journal of Chemical Information and Modeling|January 4, 2025
End-Point Affinity Estimation of Galectin Ligands by Classical and Semiempirical Quantum Mechanical PotentialsJan Choutka, Jakub Kaminský, Ercheng Wang, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|June 28, 2021
Facile Approach to C-Glucosides by Using a Protecting-Group-Free Hiyama Cross-Coupling Reaction: High-Yielding Dapagliflozin SynthesisKarolína Vaňková, Michal Rahm, Jan Choutka, et al.
Organic & Biomolecular Chemistry|July 21, 2022
Silicon-bridged (1→1)-disaccharides: an umpoled glycomimetic scaffoldJan Choutka, Michal Kratochvíl, Ivana Císařová, et al.
Pageof 2