4.8 Article

Silyl-Substituted Spirodiepoxides: Stereoselective Formation and Regioselective Opening

Journal

ORGANIC LETTERS
Volume 11, Issue 20, Pages 4672-4675

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol901948d

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Funding

  1. NIH [GM-078145]

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A short synthesis of the natural product epi-citreodiol and the method developed to gain access to this target are described. Key advances focus on silyl substituted allenes. Upon exposure to dimethyldioxirane, spirodiepoxides form with high face selectivity and subsequently react at the silyl terminus.

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