Addition Reaction of Imidazoles and Thiazoles with Silyl Enol Ethers in the Presence of Alkyl Chloroformate
โ Scribed by Takashi Itoh; Michiko Miyazaki; Kazuhiro Nagata; Akio Ohsawa
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 205 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0040-4020
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โฆ Synopsis
AbstractรSilyl enol ethers and ketene silyl acetals reacted with imidazole, thiazole, and their benzo derivatives in the presence of an alkyl chloroformate to give 2-substituted imidazolines and thiazolines in good yields via the intermediacy of unstable N-acylated quaternary salts of azoles. In addition, it was found that silyl enol ethers formed in situ were also useful for the reaction to afford the adducts only by simple sequential addition of ยฎve commercially available reagents.
๐ SIMILAR VOLUMES
## Abstract **Summary:** Vinyl ether oligomers with reactive end groups were prepared by alkylation of silyl enol ethers during propagation. Silyl enol ethers were added to the cationic polymerization of isobutyl vinyl ether, ethyl vinyl ether and methyl vinyl ether. The polymerizations were carrie
ne aldol reaction of siIyl enol ethers with aldehydes is \_wccessfuIly carried out in aqueous media by using a lanthsnide trifluoromethanesulfonate as a catalyst. Water soluble aldehydes are applicable and the catalyst can be recovered andreusedin this reaction.