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Remote Control of Diastereoselectivity in Intramolecular Reactions of Chiral Allylsilanes

During investigations of cyclization reactions between chiral allylsilanes and N-acyliminium ions, it was discovered that a suitably positioned benzyloxy group on the allylsilane component caused a reversal in the diastereoselectivity of these reactions relative to that normally observed with alkyl-...

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Autors principals: Judd, Weston R., Ban, Sooho, Aubé, Jeffrey
Format: Artigo
Idioma:Inglês
Publicat: 2006
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2519900/
https://ncbi.nlm.nih.gov/pubmed/17044701
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ja063411+
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