Additional Properties
Hydrolytic Sensitivity 7: reacts slowly with moisture/water Application Potential for the synthesis of silyl-protected butynol derivatives.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. 4-(t-Butyldimethylsi
loxy)butyne; 4-(t-Butyldimethylsi
loxy)-1-butyne
Protected butynol
Potential for the synthesis of silyl-protected butynol derivatives
Potential for the formation of TBS-protected butynols
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 7: reacts slowly with moisture/water Application Potential for the synthesis of silyl-protected butynol derivatives.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. 4-(t-Butyldimethylsi
loxy)butyne; 4-(t-Butyldimethylsi
loxy)-1-butyne
Protected butynol
Potential for the synthesis of silyl-protected butynol derivatives
Potential for the formation of TBS-protected butynols
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 7: reacts slowly with moisture/water Application Potential for the synthesis of silyl-protected butynol derivatives.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. 4-(t-Butyldimethylsi
loxy)butyne; 4-(t-Butyldimethylsi
loxy)-1-butyne
Protected butynol
Potential for the synthesis of silyl-protected butynol derivatives
Potential for the formation of TBS-protected butynols
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 7: reacts slowly with moisture/water
Application
Potential for the synthesis of silyl-protected butynol derivatives.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.
4-(t-Butyldimethylsiloxy)butyne; 4-(t-Butyldimethylsiloxy)-1-butyne
Protected butynol
Potential for the synthesis of silyl-protected butynol derivatives
Potential for the formation of TBS-protected butynols
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
