Sequential Pd(0)-catalyzed reactions for the construction of multiple substituted furans. A short synthesis of the F5 furan fatty acid1a
✍ Scribed by Thorsten Bach; Lars Krüger
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 225 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
4,5-Dibromofurfural (1) undergoes a regioselective Pd(0)-catalyzed C-C bond forming reaction at its C-5 position to yield the corresponding furans 3. The second bromine substituent in C-4 position can be substituted by a methyl group in a subsequent Pd(0)catalyzed cross coupling reaction. The furan fatty acid 12 and its benzyl ester 13 were prepared in a short synthetic sequence using this method.
📜 SIMILAR VOLUMES
synthesis of 2-aryl substituted 5-, 6-, and
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