Stannane, tributylchloro

Tributyltin chloride Stannane, tributylchloro- (8,9) (1461-22-9) Bi (triphenylphosphine)palladium(ll) chloride Palladium, dichlorobis(1riphenylphosphine)- (8,9) (13965-03-2)... 

Caswell No. 867A CCRIS 6319 Chlorid tri-n-butylcinicity Chloroln-n-butylstannane Chlorotri-n-butyltin Chlorotributylstannane Chlorotributyltin EINECS 215-958-7 EPA Pesticide Chemical Code 083107 HSDB 6816 Monochlorotributyltin NSC 22323 Stannane, chlorotributyl- Stannane, tributylchloro- Tin, tri-n-butyl-, chloride Tri-n-butylchlorotin Tri-n-butyltin chloride Tri-N-butylzinn-chlorid Tributylchlorostannane Tributylchlorotin Tributylstannium chloride Tribu l-stannyl chloride TributylSn chloride WR 3396. Registered by EPA as a fungicide (cancelled). Oil bp25 = 171-173° d = 1.20C Fluka. 

A-allylic amines are conveniently prepared in high yields by the reaction of azides with allylindium reagents in the presence of sodium iodide at ambient temperature (Equation (74)).307 Stannylation with tributylchloro-stannane occurs exclusively at the a-carbon, yielding allyltributylstannanes (E, Z)-isomerization of the allylic double bond depends largely upon the substitution pattern on the allylic moiety (Equation (75)).26 Allyl and propargyl bromides react with diphenyl diselenides in aqueous media to give allyl and propargyl selenides (Equation (76)).308 309... 

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