A Study of the Conjugate Addition of Thionucleophiles to 2(5H)-Furanones
✍ Scribed by Felix Busqué; Pedro de March; Marta Figueredo; Josep Font; Lluïsa González
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 170 KB
- Volume
- 2004
- Category
- Article
- ISSN
- 1434-193X
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📜 SIMILAR VOLUMES
A novel rearrangement of 2(SH)-furanones is described. When refluxed in aq. ethanolic solution in the presence of excess KOH, the 2,5-dihydro-2-oxofuran-3-carboxamides 6 underwent a novel rearrangement to the corresponding 4,5-dihydro-4-oxo-2-(phenylamino)-3-furancarboxylic acids 1 in moderate-to-ex
## Abstract The photochemical behaviour of the title compound **2c** was investigated in various solvents. In benzene and __t__‐butanol photodimerization affords the __cis__‐__anti__‐__cis HH__‐ and __HT__‐dimers (H = head, T = tail). In acetonitrile, cyclohexane and 2‐propanol, photoreduction comp