Additional Properties
Hydrolytic Sensitivity 4: no reaction with water under neutral conditions Application Useful in silicon-mediated Sonogashira cross-coupling reactions.1 Reference 1. Larson, G. L. “Silicon-Based Cross-Coupling Reagents” Gelest, Inc. 2011. Safety
Packaging Under Nitrogen Alkynylsilane Cross-Coupling Agent The cross-coupling reaction is a highly useful methodology for the formation of carbon-carbon bonds. It involves two reagents, with one typically being a suitable organometallic reagent - the nucleophile - and the other a suitable organic substrate, normally an unsaturated halide, tosylate or similar - the electrophile. 1,3-Diethynyltetrame
thyldisiloxane; Diethynyltetramethyl
disiloxane
End-capper for acetylene functional silicones
Useful in Sonogashira reactions
Extensive review of silicon based cross-coupling agents: Denmark, S. E. et al. "Organic Reactions, Volume 75" Denmark, S. E. ed., John Wiley and Sons, 233, 2011
Gelest, Inc.
Done
Datasheet
Description
Additional Properties
Hydrolytic Sensitivity 4: no reaction with water under neutral conditions Application Useful in silicon-mediated Sonogashira cross-coupling reactions.1 Reference 1. Larson, G. L. “Silicon-Based Cross-Coupling Reagents” Gelest, Inc. 2011. Safety
Packaging Under Nitrogen Alkynylsilane Cross-Coupling Agent The cross-coupling reaction is a highly useful methodology for the formation of carbon-carbon bonds. It involves two reagents, with one typically being a suitable organometallic reagent - the nucleophile - and the other a suitable organic substrate, normally an unsaturated halide, tosylate or similar - the electrophile. 1,3-Diethynyltetrame
thyldisiloxane; Diethynyltetramethyl
disiloxane
End-capper for acetylene functional silicones
Useful in Sonogashira reactions
Extensive review of silicon based cross-coupling agents: Denmark, S. E. et al. "Organic Reactions, Volume 75" Denmark, S. E. ed., John Wiley and Sons, 233, 2011
Additional Properties
Hydrolytic Sensitivity 4: no reaction with water under neutral conditions Application Useful in silicon-mediated Sonogashira cross-coupling reactions.1 Reference 1. Larson, G. L. “Silicon-Based Cross-Coupling Reagents” Gelest, Inc. 2011. Safety
Packaging Under Nitrogen Alkynylsilane Cross-Coupling Agent The cross-coupling reaction is a highly useful methodology for the formation of carbon-carbon bonds. It involves two reagents, with one typically being a suitable organometallic reagent - the nucleophile - and the other a suitable organic substrate, normally an unsaturated halide, tosylate or similar - the electrophile. 1,3-Diethynyltetrame
thyldisiloxane; Diethynyltetramethyl
disiloxane
End-capper for acetylene functional silicones
Useful in Sonogashira reactions
Extensive review of silicon based cross-coupling agents: Denmark, S. E. et al. "Organic Reactions, Volume 75" Denmark, S. E. ed., John Wiley and Sons, 233, 2011
Additional Properties
Hydrolytic Sensitivity 4: no reaction with water under neutral conditions
Application
Useful in silicon-mediated Sonogashira cross-coupling reactions.1
Reference
1. Larson, G. L. “Silicon-Based Cross-Coupling Reagents” Gelest, Inc. 2011.
Safety
Packaging Under Nitrogen
Alkynylsilane Cross-Coupling Agent
The cross-coupling reaction is a highly useful methodology for the formation of carbon-carbon bonds. It involves two reagents, with one typically being a suitable organometallic reagent - the nucleophile - and the other a suitable organic substrate, normally an unsaturated halide, tosylate or similar - the electrophile.
1,3-Diethynyltetramethyldisiloxane; Diethynyltetramethyldisiloxane
End-capper for acetylene functional silicones
Useful in Sonogashira reactions
Extensive review of silicon based cross-coupling agents: Denmark, S. E. et al. "Organic Reactions, Volume 75" Denmark, S. E. ed., John Wiley and Sons, 233, 2011
