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Palladium-catalyzed synthesis of 9-fluorenylidenes through aryne annulation.

ABSTRACT: The palladium-catalyzed annulation of arynes by substituted o-halostyrenes produces substituted 9-fluorenylidenes in good yields. This methodology provides this important carbocyclic ring system in a single step, which involves the generation of two new carbon-carbon bonds, occurs under relatively mild reaction conditions, and tolerates a variety of functional groups, including cyano, ester, aldehyde, and ketone groups.

SUBMITTER: Worlikar SA

PROVIDER: S-EPMC2731569 | biostudies-literature | 2009 Jun

REPOSITORIES: biostudies-literature

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Palladium-catalyzed synthesis of 9-fluorenylidenes through aryne annulation.

Worlikar Shilpa A SA Larock Richard C RC

Organic letters 20090601 11

The palladium-catalyzed annulation of arynes by substituted o-halostyrenes produces substituted 9-fluorenylidenes in good yields. This methodology provides this important carbocyclic ring system in a single step, which involves the generation of two new carbon-carbon bonds, occurs under relatively mild reaction conditions, and tolerates a variety of functional groups, including cyano, ester, aldehyde, and ketone groups. ...[more]

PMID: 19413328

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