Abstract
Under the acidic conditions, substituted furans were constructed from γ-alkynyl ketones through corresponding allene intermediates in one-pot. The methodology was also tailored to a series of the Ugi reaction products for the synthesis of 6-methylpyrazin-2(1H)-one derivatives. The current method offered significant advantages for the combinatorial applications of these chemical scaffolds.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 292-297 |
| Number of pages | 6 |
| Journal | ACS Combinatorial Science |
| Volume | 20 |
| Issue number | 5 |
| DOIs | |
| State | Published - May 14 2018 |
Keywords
- 6-methylpyrazin-2(1 H)-one
- Ugi reaction
- allene
- multicomponent reaction (MCR)
- substituted furans
ASJC Scopus subject areas
- General Chemistry
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