The effectiveness of cationic species for increasing the catalytic activity of organotin Lewis acids has been assessed by comparing two types of cationic organotin clusters, [Bu 2 Sn(OH)(H 2 O)] 2 2+ 2OTf - and [(BuSn) 12 O 14 (OH) 6 ] 2+ Cl - 2 ·2H 2 O, with neutral clusters in alcohol acetylation. The Sn 2 dication is extremely active, with a catalyst concentration of 0.001 mol %, sufficient to give a quantitative yield. The Sn 12 dication is slightly less active but gives high levels of chemoselectivity and primary/secondary alcohols selection. The neutral clusters are less effective catalysts. A variety of synthetic applications are feasible by changing the Lewis acidity of the catalysts.
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Durand et al. (2000) studied this question.
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