Additional Properties
Hydrolytic Sensitivity 1: no significant reaction with aqueous systems Application Polymerizes perfluoroalkylacetyl
enes in combination with WCl6.1 Cocatalyst with NbCl5 for trimerization-cycliz
ation of diynes.2 Reference 1. Tsuchihara, K. et al. Chem. Abstr. 110, 95877t; Polym. Bull. 1988, 20(4), 343. 2. Srinivasan, R. et al. J. Mol. Catal. 1989, 53, 203. Safety
Packaging Under Nitrogen Organotin 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. Tetraphenyltin; Tetraphenylstannane
Stille Coupling phenylation reagent
Polymerizes perfluoroalkylacetyl
enes in combination with WCl6
Cocatalyst with NbCl5 for trimerization-cycliz
ation of diynes
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 1: no significant reaction with aqueous systems Application Polymerizes perfluoroalkylacetyl
enes in combination with WCl6.1 Cocatalyst with NbCl5 for trimerization-cycliz
ation of diynes.2 Reference 1. Tsuchihara, K. et al. Chem. Abstr. 110, 95877t; Polym. Bull. 1988, 20(4), 343. 2. Srinivasan, R. et al. J. Mol. Catal. 1989, 53, 203. Safety
Packaging Under Nitrogen Organotin 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. Tetraphenyltin; Tetraphenylstannane
Stille Coupling phenylation reagent
Polymerizes perfluoroalkylacetyl
enes in combination with WCl6
Cocatalyst with NbCl5 for trimerization-cycliz
ation of diynes
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 1: no significant reaction with aqueous systems Application Polymerizes perfluoroalkylacetyl
enes in combination with WCl6.1 Cocatalyst with NbCl5 for trimerization-cycliz
ation of diynes.2 Reference 1. Tsuchihara, K. et al. Chem. Abstr. 110, 95877t; Polym. Bull. 1988, 20(4), 343. 2. Srinivasan, R. et al. J. Mol. Catal. 1989, 53, 203. Safety
Packaging Under Nitrogen Organotin 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. Tetraphenyltin; Tetraphenylstannane
Stille Coupling phenylation reagent
Polymerizes perfluoroalkylacetyl
enes in combination with WCl6
Cocatalyst with NbCl5 for trimerization-cycliz
ation of diynes
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 1: no significant reaction with aqueous systems
Application
Polymerizes perfluoroalkylacetylenes in combination with WCl6.1 Cocatalyst with NbCl5 for trimerization-cyclization of diynes.2
Reference
1. Tsuchihara, K. et al. Chem. Abstr. 110, 95877t; Polym. Bull. 1988, 20(4), 343. 2. Srinivasan, R. et al. J. Mol. Catal. 1989, 53, 203.
Safety
Packaging Under Nitrogen
Organotin 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.
Tetraphenyltin; Tetraphenylstannane
Stille Coupling phenylation reagent
Polymerizes perfluoroalkylacetylenes in combination with WCl6
Cocatalyst with NbCl5 for trimerization-cyclization of diynes
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
