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Intermolecular silacarbonyl ylide cycloadditions: a direct pathway to oxasilacyclopentenes.


ABSTRACT: Silacarbonyl ylides, generated by metal-catalyzed silylene transfer to carbonyls, participate in formal intermolecular 1,3-dipolar cycloaddition reactions with carbonyl compounds and alkynes to form dioxasilacyclopentane acetals and oxasilacyclopentenes in an efficient, one-step process.

SUBMITTER: Bourque LE 

PROVIDER: S-EPMC2664292 | biostudies-literature | 2008 Nov

REPOSITORIES: biostudies-literature

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Intermolecular silacarbonyl ylide cycloadditions: a direct pathway to oxasilacyclopentenes.

Bourque Laura E LE   Woerpel K A KA  

Organic letters 20081016 22


Silacarbonyl ylides, generated by metal-catalyzed silylene transfer to carbonyls, participate in formal intermolecular 1,3-dipolar cycloaddition reactions with carbonyl compounds and alkynes to form dioxasilacyclopentane acetals and oxasilacyclopentenes in an efficient, one-step process. ...[more]

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