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[摘要]:Silylene transfer to allylic sulfides results in a formal 1,2-sulfide migration. The rearrangement yields substituted silacyclobutanes, not the expected silacyclopropanes. The silacyclobutanes were elaborated by insertions of carbonyl compounds selectively into one carbon silicon bond. A mechanism for the 1,2-sulfide migration is proposed involving an episulfonium ion intermediate. |
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