## Abstract The α‐thiotetronic acid 1 reacts with amines predominantly with ring opening to give polyfunctionalized ketones (2) which readily cyclize to α‐tetramic acid amides (4a, b). The reaction of α‐thiotetronate 6 with nucleophiles is more complex, leading to either an open‐chain derivative (8
✦ LIBER ✦
ChemInform Abstract: α-Thiotetronic Acids. Part 2. Reactions of γ-Alkylidene-. alpha.-thiotetronic Acids.
✍ Scribed by H.-D. STACHEL; K. ZEITLER
- Book ID
- 112027597
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 39 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0931-7597
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