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The Journal of Organic Chemistry
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August 12, 2008
Nucleophilicity and leaving-group ability in frontside and backside S(N)2 reactions
A Patrícia Bento, F Matthias Bickelhaupt
Chemistry, an Asian Journal
|
August 21, 2008
Frontside versus Backside S(N)2 substitution at group 14 atoms: origin of reaction barriers and reasons for their absence
A Patrícia Bento, F Matthias Bickelhaupt
The Journal of Organic Chemistry
|
February 16, 2007
Nucleophilic substitution at silicon (SN2@Si) via a central reaction barrier
A Patrícia Bento, F Matthias Bickelhaupt
Journal of Chemical Theory and Computation
|
December 2, 2015
E2 and SN2 Reactions of X(-) + CH3CH2X (X = F, Cl); an ab Initio and DFT Benchmark Study
A Patrícia Bento, Miquel Solà, F Matthias Bickelhaupt
Journal of Computational Chemistry
|
August 11, 2005
Ab initio and DFT benchmark study for nucleophilic substitution at carbon (SN2@C) and silicon (SN2@Si)
A Patrícia Bento, Miquel Solà, F Matthias Bickelhaupt
Drug Discovery Today. Technologies
|
July 22, 2015
Chemical databases: curation or integration by user-defined equivalence?
Anne Hersey, Jon Chambers, Louisa Bellis, et al.
Chemical Research in Toxicology
|
January 28, 2021
Drug Safety Data Curation and Modeling in ChEMBL: Boxed Warnings and Withdrawn Drugs
Fiona M I Hunter, A Patrícia Bento, Nicolas Bosc, et al.
Journal of Biomedical Semantics
|
September 29, 2016
A drug target slim: using gene ontology and gene ontology annotations to navigate protein-ligand target space in ChEMBL
Prudence Mutowo, A Patrícia Bento, Nathan Dedman, et al.
Drug Discovery Today
|
August 24, 2010
Ligand efficiency indices for an effective mapping of chemico-biological space: the concept of an atlas-like representation
Cele Abad-Zapatero, Ognjen Perišić, John Wass, et al.
Scientific Data
|
October 24, 2018
A large-scale dataset of in vivo pharmacology assay results
Fiona M I Hunter, Francis L Atkinson, A Patrícia Bento, et al.
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of 3
Search research articles
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Showing results (1-10 of 22) with videos related to
Sort By:
Page
of 3
The Journal of Organic Chemistry
|
August 12, 2008
Nucleophilicity and leaving-group ability in frontside and backside S(N)2 reactions
A Patrícia Bento, F Matthias Bickelhaupt
Chemistry, an Asian Journal
|
August 21, 2008
Frontside versus Backside S(N)2 substitution at group 14 atoms: origin of reaction barriers and reasons for their absence
A Patrícia Bento, F Matthias Bickelhaupt
The Journal of Organic Chemistry
|
February 16, 2007
Nucleophilic substitution at silicon (SN2@Si) via a central reaction barrier
A Patrícia Bento, F Matthias Bickelhaupt
Journal of Chemical Theory and Computation
|
December 2, 2015
E2 and SN2 Reactions of X(-) + CH3CH2X (X = F, Cl); an ab Initio and DFT Benchmark Study
A Patrícia Bento, Miquel Solà, F Matthias Bickelhaupt
Journal of Computational Chemistry
|
August 11, 2005
Ab initio and DFT benchmark study for nucleophilic substitution at carbon (SN2@C) and silicon (SN2@Si)
A Patrícia Bento, Miquel Solà, F Matthias Bickelhaupt
Drug Discovery Today. Technologies
|
July 22, 2015
Chemical databases: curation or integration by user-defined equivalence?
Anne Hersey, Jon Chambers, Louisa Bellis, et al.
Chemical Research in Toxicology
|
January 28, 2021
Drug Safety Data Curation and Modeling in ChEMBL: Boxed Warnings and Withdrawn Drugs
Fiona M I Hunter, A Patrícia Bento, Nicolas Bosc, et al.
Journal of Biomedical Semantics
|
September 29, 2016
A drug target slim: using gene ontology and gene ontology annotations to navigate protein-ligand target space in ChEMBL
Prudence Mutowo, A Patrícia Bento, Nathan Dedman, et al.
Drug Discovery Today
|
August 24, 2010
Ligand efficiency indices for an effective mapping of chemico-biological space: the concept of an atlas-like representation
Cele Abad-Zapatero, Ognjen Perišić, John Wass, et al.
Scientific Data
|
October 24, 2018
A large-scale dataset of in vivo pharmacology assay results
Fiona M I Hunter, Francis L Atkinson, A Patrícia Bento, et al.
Page
of 3