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Silyl-substituted spirodiepoxides: stereoselective formation and regioselective opening.

ABSTRACT: 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.

SUBMITTER: Ghosh P

PROVIDER: S-EPMC3047402 | biostudies-literature | 2009 Oct

REPOSITORIES: biostudies-literature

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Silyl-substituted spirodiepoxides: stereoselective formation and regioselective opening.

Ghosh Partha P Cusick Joseph R JR Inghrim Jennifer J Williams Lawrence J LJ

Organic letters 20091001 20

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. ...[more]

PMID: 19810767

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