A new synthesis of alkyl 1-alkyl-2-methylpyrrole-3-carboxylates by ring transformation of 2-chloro-2-acetimidoylbutyrolactones
β Scribed by Bart Kesteleyn; Erick Rosas Alonso; Christian Stevens; Yves Dejaegher; Maria Peristeropoulou; Tuyen Nguyen Van; Oleg Kulinkovich; Norbert De Kimpe
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 851 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0040-4020
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β¦ Synopsis
Reaction of 2-chloro-2-acetimidoylbutyrolactones with sodium methoxide or sodium ethoxide in the corresponding alcohol provides a facile one-step synthesis of methyl or ethyl l-alkyl-2methylpyrrole-3-carboxylates from readily available starting materials.
π SIMILAR VOLUMES
Aziridines / Oxazolines / Ring expansion reactions / Ξ±-Hydroxy Ξ²-amino acids / Ξ²-Hydroxy Ξ±-amino acids A new method for the preparation of 2,2,3-trisubstituted methyl 1-benzoylaziridine-2-carboxylates is reported. These compounds have been obtained starting from Ξ±-alkyl Ξ²amino acids by formation of