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Jonathan M Percy

Showing results (41-50 of 46) with videos related to

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Organic & Biomolecular Chemistry|February 11, 2004
Highly-functionalised difluorinated (hydroxymethyl)conduritol analogues via the Diels-Alder reactions of a difluorinated dienophileAndrea Arany, Patrick J Crowley, John Fawcett, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|July 15, 2016
Modular Construction of Fluoroarenes from a New Difluorinated Building Block by Cross-Coupling/Electrocyclisation/Dehydrofluorination ReactionsJonathan M Percy, Helena Emerson, James W B Fyfe, et al.
Organic & Biomolecular Chemistry|February 20, 2009
Sugar nucleotide recognition by Klebsiella pneumoniae UDP-D-galactopyranose mutase: fluorinated substrates, kinetics and equilibriaJames C Errey, Maretta C Mann, Shirley A Fairhurst, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|October 6, 2011
Why is RCM favoured over dimerisation? Predicting and estimating thermodynamic effective molarities by solution experiments and electronic structure calculationsDavid J Nelson, Ian W Ashworth, Ian H Hillier, et al.
Bioorganic & Medicinal Chemistry|June 10, 2014
Lead identification of benzimidazolone and azabenzimidazolone arylsulfonamides as CC-chemokine receptor 4 (CCR4) antagonistsAfjal H Miah, Hossay Abas, Malcolm Begg, et al.
European Journal of Medicinal Chemistry|March 19, 2016
2,8-Diazaspiro[4.5]decan-8-yl)pyrimidin-4-amine potent CCR4 antagonists capable of inducing receptor endocytosisLena Shukla, Laura A Ajram, Malcolm Begg, et al.
Pageof 5

Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 46 results.
Organic & Biomolecular Chemistry|February 11, 2004
Highly-functionalised difluorinated (hydroxymethyl)conduritol analogues via the Diels-Alder reactions of a difluorinated dienophileAndrea Arany, Patrick J Crowley, John Fawcett, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|July 15, 2016
Modular Construction of Fluoroarenes from a New Difluorinated Building Block by Cross-Coupling/Electrocyclisation/Dehydrofluorination ReactionsJonathan M Percy, Helena Emerson, James W B Fyfe, et al.
Organic & Biomolecular Chemistry|February 20, 2009
Sugar nucleotide recognition by Klebsiella pneumoniae UDP-D-galactopyranose mutase: fluorinated substrates, kinetics and equilibriaJames C Errey, Maretta C Mann, Shirley A Fairhurst, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|October 6, 2011
Why is RCM favoured over dimerisation? Predicting and estimating thermodynamic effective molarities by solution experiments and electronic structure calculationsDavid J Nelson, Ian W Ashworth, Ian H Hillier, et al.
Bioorganic & Medicinal Chemistry|June 10, 2014
Lead identification of benzimidazolone and azabenzimidazolone arylsulfonamides as CC-chemokine receptor 4 (CCR4) antagonistsAfjal H Miah, Hossay Abas, Malcolm Begg, et al.
European Journal of Medicinal Chemistry|March 19, 2016
2,8-Diazaspiro[4.5]decan-8-yl)pyrimidin-4-amine potent CCR4 antagonists capable of inducing receptor endocytosisLena Shukla, Laura A Ajram, Malcolm Begg, et al.
Pageof 5