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Johan M Winne

Showing results (41-50 of 56) with videos related to

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Chemical Reviews|February 23, 2016
Triazolinediones as Highly Enabling Synthetic ToolsKevin De Bruycker, Stijn Billiet, Hannes A Houck, et al.
Chemical Science|September 22, 2023
Site selective gold(i)-catalysed benzylic C-H amination <i>via</i> an intermolecular hydride transfer to triazolinedionesKevin Bevernaege, Nikolaos V Tzouras, Albert Poater, et al.
Chemical Science|June 3, 2022
Triazolinedione protein modification: from an overlooked off-target effect to a tryptophan-based bioconjugation strategyKlaas W Decoene, Kamil Unal, An Staes, et al.
Angewandte Chemie (International Ed. in English)|December 26, 2024
Tailoring the Reprocessability of Thiol-Ene Networks through Ring Size EffectsVincent Scholiers, Susanne M Fischer, Bram Daelman, et al.
Nature Chemistry|August 22, 2014
Triazolinediones enable ultrafast and reversible click chemistry for the design of dynamic polymer systemsStijn Billiet, Kevin De Bruycker, Frank Driessen, et al.
The Journal of Organic Chemistry|January 24, 2015
Possibility of [1,5] sigmatropic shifts in bicyclo[4.2.0]octa-2,4-dienesHannelore Goossens, Johan M Winne, Sebastian Wouters, et al.
Nature Communications|July 10, 2025
Thiol-thiol cross-clicking using bromo-ynone reagentsMarvin Nicque, Jan H Meffert, Diederick Maes, et al.
Organic Letters|January 3, 2022
Correction to "Regio- and Stereoselective Synthesis of C-4' Spirocyclobutyl Ribofuranose Scaffolds and Their Use as Biologically Active Nucleoside Analogues"Lucile Jouffroy, Jonas Verhoeven, Marta Brambilla, et al.
Organic Letters|November 3, 2021
Regio- and Stereoselective Synthesis of C-4' Spirocyclobutyl Ribofuranose Scaffolds and Their Use as Biologically Active Nucleoside AnaloguesLucile Jouffroy, Jonas Verhoeven, Marta Brambilla, et al.
Chemical Science|April 30, 2025
Eliminating creep in vitrimers using temperature-resilient siloxane exchange chemistry and N-heterocyclic carbenesTapas Debsharma, Loc Tan Nguyen, Benon P Maliszewski, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
Chemical Reviews|February 23, 2016
Triazolinediones as Highly Enabling Synthetic ToolsKevin De Bruycker, Stijn Billiet, Hannes A Houck, et al.
Chemical Science|September 22, 2023
Site selective gold(i)-catalysed benzylic C-H amination <i>via</i> an intermolecular hydride transfer to triazolinedionesKevin Bevernaege, Nikolaos V Tzouras, Albert Poater, et al.
Chemical Science|June 3, 2022
Triazolinedione protein modification: from an overlooked off-target effect to a tryptophan-based bioconjugation strategyKlaas W Decoene, Kamil Unal, An Staes, et al.
Angewandte Chemie (International Ed. in English)|December 26, 2024
Tailoring the Reprocessability of Thiol-Ene Networks through Ring Size EffectsVincent Scholiers, Susanne M Fischer, Bram Daelman, et al.
Nature Chemistry|August 22, 2014
Triazolinediones enable ultrafast and reversible click chemistry for the design of dynamic polymer systemsStijn Billiet, Kevin De Bruycker, Frank Driessen, et al.
The Journal of Organic Chemistry|January 24, 2015
Possibility of [1,5] sigmatropic shifts in bicyclo[4.2.0]octa-2,4-dienesHannelore Goossens, Johan M Winne, Sebastian Wouters, et al.
Nature Communications|July 10, 2025
Thiol-thiol cross-clicking using bromo-ynone reagentsMarvin Nicque, Jan H Meffert, Diederick Maes, et al.
Organic Letters|January 3, 2022
Correction to "Regio- and Stereoselective Synthesis of C-4' Spirocyclobutyl Ribofuranose Scaffolds and Their Use as Biologically Active Nucleoside Analogues"Lucile Jouffroy, Jonas Verhoeven, Marta Brambilla, et al.
Organic Letters|November 3, 2021
Regio- and Stereoselective Synthesis of C-4' Spirocyclobutyl Ribofuranose Scaffolds and Their Use as Biologically Active Nucleoside AnaloguesLucile Jouffroy, Jonas Verhoeven, Marta Brambilla, et al.
Chemical Science|April 30, 2025
Eliminating creep in vitrimers using temperature-resilient siloxane exchange chemistry and N-heterocyclic carbenesTapas Debsharma, Loc Tan Nguyen, Benon P Maliszewski, et al.
Pageof 6