Éric Fouquet , Michel Pereyre , Jean-Claude Rayez , Marie-Thérèse Rayez , Thomas Roulet
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引用次数: 1
Abstract
We have previously highlighted the ability of the N,N-bistrimethylsilylaminostannylene 1 to produce monoallylstannanes 2 in quantitative yields, starting from various functionalised allylic halides via an insertion reaction. In contrast with more electrophilic trihalogenotin radicals, the tin-centred radicals generated from reagents 2 are shown to be the best candidates towards allylic radical transfer, giving allylated products in similar yields as those obtained with classical tributyltin radicals.
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