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Magnus Liljenberg

Showing results (1-10 of 6) with videos related to

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Chemical Research in Toxicology|October 20, 2020
Theoretical Studies of the Mechanism of Carbamoylation of Nucleobases by IsocyanatesMagnus Liljenberg, Lena Ripa, Igor Shamovsky
The Journal of Physical Chemistry. A|March 6, 2018
Theoretical Investigation into Rate-Determining Factors in Electrophilic Aromatic HalogenationMagnus Liljenberg, Joakim Halldin Stenlid, Tore Brinck
Journal of Molecular Modeling|December 20, 2017
Mechanism and regioselectivity of electrophilic aromatic nitration in solution: the validity of the transition state approachMagnus Liljenberg, Joakim Halldin Stenlid, Tore Brinck
Beilstein Journal of Organic Chemistry|June 15, 2013
Utilizing the σ-complex stability for quantifying reactivity in nucleophilic substitution of aromatic fluoridesMagnus Liljenberg, Tore Brinck, Tobias Rein, et al.
The Journal of Organic Chemistry|March 6, 2012
Predicting regioselectivity in nucleophilic aromatic substitutionMagnus Liljenberg, Tore Brinck, Björn Herschend, et al.
The Journal of Organic Chemistry|June 18, 2010
Validation of a computational model for predicting the site for electrophilic substitution in aromatic systemsMagnus Liljenberg, Tore Brinck, Björn Herschend, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Chemical Research in Toxicology|October 20, 2020
Theoretical Studies of the Mechanism of Carbamoylation of Nucleobases by IsocyanatesMagnus Liljenberg, Lena Ripa, Igor Shamovsky
The Journal of Physical Chemistry. A|March 6, 2018
Theoretical Investigation into Rate-Determining Factors in Electrophilic Aromatic HalogenationMagnus Liljenberg, Joakim Halldin Stenlid, Tore Brinck
Journal of Molecular Modeling|December 20, 2017
Mechanism and regioselectivity of electrophilic aromatic nitration in solution: the validity of the transition state approachMagnus Liljenberg, Joakim Halldin Stenlid, Tore Brinck
Beilstein Journal of Organic Chemistry|June 15, 2013
Utilizing the σ-complex stability for quantifying reactivity in nucleophilic substitution of aromatic fluoridesMagnus Liljenberg, Tore Brinck, Tobias Rein, et al.
The Journal of Organic Chemistry|March 6, 2012
Predicting regioselectivity in nucleophilic aromatic substitutionMagnus Liljenberg, Tore Brinck, Björn Herschend, et al.
The Journal of Organic Chemistry|June 18, 2010
Validation of a computational model for predicting the site for electrophilic substitution in aromatic systemsMagnus Liljenberg, Tore Brinck, Björn Herschend, et al.
Pageof 1