Ketenedithioacetals as Surrogates for the Formal Insertion of Ketenes into Donor–Acceptor Cyclopropanes

Volume: 2020, Issue: 17, Pages: 2560 - 2564
Published: Apr 15, 2020
Abstract
The reactivity of donor–acceptor (D–A) cyclopropanes towards acceptor‐substituted ketenedithioacetals was investigated. In a Lewis‐acid‐catalyzed (3+2)‐cycloaddition, the corresponding dithiaspiro compounds were synthesized in good yields. The 1,3‐dithiane unit, a masked keto functionality, was cleaved by N ‐iodosuccinimide. Thus, this two‐step process represents a formal insertion of an acceptor‐substituted ketene into a D–A...
Paper Details
Title
Ketenedithioacetals as Surrogates for the Formal Insertion of Ketenes into Donor–Acceptor Cyclopropanes
Published Date
Apr 15, 2020
Volume
2020
Issue
17
Pages
2560 - 2564
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