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Investigations on organo-tin compounds. I. The preparation of butyltin compounds by a Wurtz reaction

✍ Scribed by Van Kerk, G. J. M. Der; Luijten, J. G. A.


Book ID
120033290
Publisher
Wiley (John Wiley & Sons)
Year
2007
Weight
575 KB
Volume
4
Category
Article
ISSN
0021-8871

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📜 SIMILAR VOLUMES


Investigations on organo-tin compounds.
✍ van der Kerk, G. J. M. ;Noltes, J. G. ;Luijten, J. G. A. 📂 Article 📅 2007 🏛 Wiley (John Wiley & Sons) ⚖ 345 KB

## Abstract The preparation, according to the slightly modified procedure of Finholt __et al.__, of the following organo‐tin hydrides is described: triethyltin hydride, tri‐__n__‐propyltin hydride, tri‐__n__‐butyltin hydride, triphenyltin hydride, di‐__n__‐propyltin dihydride, di‐__n__‐butyltin dih

Investigations on organo-tin compounds.
✍ van der Kerk, G. J. M. ;Luijten, J. G. A. 📂 Article 📅 2007 🏛 Wiley (John Wiley & Sons) ⚖ 530 KB

## Abstract The preparation and properties are described of some di‐__n__‐hexyl‐, di‐__n__‐octyl‐, bis‐(2‐ethyl‐__n__‐hexyl)‐and bis‐(3 : 5 : 5‐trimethyl‐__n__‐hexyl)tin compounds, potentially interesting as non‐toxic stabilizers for vinyl plastics. An improved procedure is given for the determina

Investigations on organo-tin compounds.
✍ van der Kerk, G. J. M. ;Noltes, J. G. ;Luijten, J. G. A. 📂 Article 📅 2007 🏛 Wiley (John Wiley & Sons) ⚖ 853 KB

## Abstract A new method for the synthesis of tin‐carbon bonds is described. The synthesis involves the non‐catalysed addition of organo‐tin hydrides to olefinic double bonds at moderate temperatures (60–100°). This method allows the preparation of a variety of hitherto unknown types of functionall

Investigations on organotin compounds XI
✍ J. G. A. Luijten; G. J. M. van der Kerk 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 373 KB

## Abstract Procedures are given for the preparation of 20 organotin compounds in which a trialkyl‐ or triphenyltin group is bound to nitrogen in pyrrole, pyrazole, benzpyrazole, imidazole, 1,2,4‐triazole, benzimidazole, 1,2,3‐benztriazole, 1,2,3‐triazole and 3‐amino‐1,2,4‐triazole. In addition, th