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Diorganotin dihydrides reactions

An early example for the direct coupling of a tin reagent to Amberlite XE 305, a macroporous polystyrene, was reported by Crosby and coworkers157. The synthetic route is shown in Scheme 35. Reaction of the polymer-supported diorganotin dihydride 70 with iodooctane to give octane indicated a minimum content of 2 mmol tin hydride per gram of the polymer. [Pg.1580]

The synthesis of tristannanes and linear tetrastannanes can be achieved in a straightforward manner by employing the hydrostannolysis reaction and diorganotin dihydrides (26) and 1,1,2,2-tetraorganodistannanes (9) according to Eq. (8) 49). As shown, this methodology can be used to... [Pg.205]

In an interesting extension of the above reactions, diorganotin dihydrides have been treated with amines to obtain cyclic polytin compounds 159,188, 192, 194a, 236, 236b, 236c). In one reported case 18S) a 94% yield of octadecaethylcyclononatin was obtained from diethyltin dihydride and a pyridine-diethyltin dichloride complex. It is apparently also possible to obtain straight-chain products with suitable reagents. [Pg.51]

A potentially quite useful synthetic method was recently reported by Sawyer and Kuivila 240-242), who treated diorganotin dihydrides with carboxylic acids to obtain functionally substituted ditin compounds. Thus, the reaction of dibutyltin dihydride with acetic acid leads to 1,2-diacetoxy-tetra-n-butylditin in 65% yield. [Pg.52]

I Reaction of diorganotin dihydride with bis(tributyltin)sulfide,... [Pg.752]


See other pages where Diorganotin dihydrides reactions is mentioned: [Pg.69]    [Pg.475]    [Pg.69]    [Pg.221]    [Pg.60]    [Pg.204]    [Pg.193]   
See also in sourсe #XX -- [ Pg.475 ]




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