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Danijela Barić

Showing results (1-10 of 35) with videos related to

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ACS Omega|September 26, 2019
Utilizing the Azaazulene Scaffolds in the Design of New Organic SuperbasesDanijela Barić
The Journal of Organic Chemistry|March 1, 2013
Design of superbasic guanidines: the role of multiple intramolecular hydrogen bondsDanijela Barić, Ivan Dragičević, Borislav Kovačević
International Journal of Injury Control and Safety Promotion|July 5, 2017
Introducing experiment in pedestrian behaviour and risk perception study at urban level crossingDanijela Barić, Hrvoje Pilko, Martin Starčević
The Journal of Physical Chemistry. A|August 18, 2006
Clar's sextet rule is a consequence of the sigma-electron frameworkZvonimir B Maksić, Danijela Barić, Thomas Müller
International Journal of Molecular Sciences|June 13, 2025
Phosphazenyl Phosphine Proton Sponges: Does the Proton-Chelating Effect Enhance Their Basicity?Zoran Glasovac, Danijela Barić, Ines Despotović, et al.
The Journal of Physical Chemistry. A|July 13, 2006
A novel approach in analyzing aromaticity by homo- and isostructural reactions: an ab initio study of fluorobenzenesDanijela Barić, Borislav Kovacević, Zvonimir B Maksić, et al.
Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry|October 27, 2004
The origin of aromaticity: important role of the sigma framework in benzeneBorislav Kovacević, Danijela Barić, Zvonimir B Maksić, et al.
Organic Letters|November 5, 2019
Basicity Enhancement by Multiple Intramolecular Hydrogen Bonding in Organic Superbase <i>N</i>,<i>N</i>',<i>N</i>″,<i>N</i>‴-Tetrakis(3-(dimethylamino)propyl)triaminophosphazeneSebastian Ullrich, Danijela Barić, Xiulan Xie, et al.
Chemical Communications (Cambridge, England)|February 13, 2026
Protonated bisphosphines: a new class of powerful hydride donors capable of CO<sub>2</sub> reductionDanijela Barić, Mario Damjanović, Zoran Glasovac, et al.
International Journal of Molecular Sciences|July 13, 2024
Cholinesterase Inhibition and Antioxidative Capacity of New Heteroaromatic Resveratrol Analogs: Synthesis and Physico-Chemical PropertiesMilena Mlakić, Stanislava Talić, Ilijana Odak, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
ACS Omega|September 26, 2019
Utilizing the Azaazulene Scaffolds in the Design of New Organic SuperbasesDanijela Barić
The Journal of Organic Chemistry|March 1, 2013
Design of superbasic guanidines: the role of multiple intramolecular hydrogen bondsDanijela Barić, Ivan Dragičević, Borislav Kovačević
International Journal of Injury Control and Safety Promotion|July 5, 2017
Introducing experiment in pedestrian behaviour and risk perception study at urban level crossingDanijela Barić, Hrvoje Pilko, Martin Starčević
The Journal of Physical Chemistry. A|August 18, 2006
Clar's sextet rule is a consequence of the sigma-electron frameworkZvonimir B Maksić, Danijela Barić, Thomas Müller
International Journal of Molecular Sciences|June 13, 2025
Phosphazenyl Phosphine Proton Sponges: Does the Proton-Chelating Effect Enhance Their Basicity?Zoran Glasovac, Danijela Barić, Ines Despotović, et al.
The Journal of Physical Chemistry. A|July 13, 2006
A novel approach in analyzing aromaticity by homo- and isostructural reactions: an ab initio study of fluorobenzenesDanijela Barić, Borislav Kovacević, Zvonimir B Maksić, et al.
Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry|October 27, 2004
The origin of aromaticity: important role of the sigma framework in benzeneBorislav Kovacević, Danijela Barić, Zvonimir B Maksić, et al.
Organic Letters|November 5, 2019
Basicity Enhancement by Multiple Intramolecular Hydrogen Bonding in Organic Superbase <i>N</i>,<i>N</i>',<i>N</i>″,<i>N</i>‴-Tetrakis(3-(dimethylamino)propyl)triaminophosphazeneSebastian Ullrich, Danijela Barić, Xiulan Xie, et al.
Chemical Communications (Cambridge, England)|February 13, 2026
Protonated bisphosphines: a new class of powerful hydride donors capable of CO<sub>2</sub> reductionDanijela Barić, Mario Damjanović, Zoran Glasovac, et al.
International Journal of Molecular Sciences|July 13, 2024
Cholinesterase Inhibition and Antioxidative Capacity of New Heteroaromatic Resveratrol Analogs: Synthesis and Physico-Chemical PropertiesMilena Mlakić, Stanislava Talić, Ilijana Odak, et al.
Pageof 4