Catalytic Alkynylation of Ketones and Aldehydes Using Quaternary Ammonium Hydroxide Base

Catalytic alkynylation of diverse ketones and aldehydes using nonmetallic benzyltrimethylammonium hydroxide or a basic resin of the hydroxide type in DMSO is described. Aliphatic or alicyclic carbonyl partners gave satisfactory results, whereas aromatic ones afforded products with low yields. When a...

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Veröffentlicht in:Journal of organic chemistry 2003-05, Vol.68 (9), p.3702-3705
Hauptverfasser: Ishikawa, Teruhiko, Mizuta, Tomohiro, Hagiwara, Kumiko, Aikawa, Toshiaki, Kudo, Takayuki, Saito, Seiki
Format: Artikel
Sprache:eng
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Zusammenfassung:Catalytic alkynylation of diverse ketones and aldehydes using nonmetallic benzyltrimethylammonium hydroxide or a basic resin of the hydroxide type in DMSO is described. Aliphatic or alicyclic carbonyl partners gave satisfactory results, whereas aromatic ones afforded products with low yields. When aromatic aldehydes were reacted with phenylacetylene, enones such as chalcone derivatives were obtained in place of ynols. These organobase-catalyzed systems provide a practical nonmetallic protocol for C−C bond formation.
ISSN:0022-3263
1520-6904
DOI:10.1021/jo026592g