Three-Component Reaction of an Isocyanide and a Dialkyl Acetylenedicarboxylate with a Phenacyl Halide in the Presence of Water: An Efficient Method for the One-Pot Synthesis of γ-Iminolactone Derivatives
✍ Scribed by Ali Ramazani; Aram Rezaei; Amir Tofangchi Mahyari; Morteza Rouhani; Mehdi Khoobi
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- German
- Weight
- 138 KB
- Volume
- 93
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
The zwitterion, formed from the reaction of an alkyl isocyanide and a dialkyl acetylenedicarboxylate, reacts with phenacyl halides in H 2 O to produce g-iminolactone derivatives in high yields. H 2 O helps to avoid the use of highly toxic and environmentally unfavorable solvents for this conversion.
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