Configuration??Dependent Ring Opening of Silyloxiranes: Synthesis of Functionalized Alkenes or Tetrahydrofurans
J Lange, E Schaumann
Index: Lange, Jens; Schaumann, Ernst European Journal of Organic Chemistry, 2009 , # 27 p. 4674 - 4684
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Abstract
Abstract cis-and trans-Silyloxiranes with a potential tosylate or bromide leaving group in the β position are available by the diastereospecific reduction of the corresponding alkynes with DIBAL-H and hydrosilylation with silanes, respectively. In the reaction with the anion of a silylthioacetal, the outcome of the reaction is configuration dependent: the cis-oxiranes add nucleophilic methanthiolate and give a cis-vinyl sulfide unit in a Peterson olefination. In ...
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