Self-assembly of pyrrole-2-carboxylates: Substituent effect on the synthon conversion
✍ Scribed by Yimei Cui; Zhenming Yin; Li Dong; Jiaqi He
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- English
- Weight
- 870 KB
- Volume
- 938
- Category
- Article
- ISSN
- 0022-2860
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
In this study, the UV induced photochemical reactions of two 2H-azirines -methyl 2-chloro-3-methyl-2H-azirine-2-carboxylate (MCMAC) and methyl 3-methyl-2H-azirine-2-carboxylate (MMAC) -isolated in argon matrices are compared. For both compounds, irradiation with > 235 nm led to observation of two pr
The FT-IR, FT-Raman and 1 H and 13 C NMR spectra of pyrrole-2-carboxylic acid (PCA) and lithium, sodium, potassium, rubidium and caesium pyrrole-2-carboxylates were recorded, assigned and compared in the Li ? Na ? K ? Rb ? Cs salt series. The effect of alkali metal ions on the electronic system of l
## Abstract Reactions of 1__H__‐pyrrole‐2,3‐diones 2a‐i with N‐ and O‐nucleophiles proceed by initial attack at C‐2 or/and C‐5. Consequently, earlier results suggesting structures of type A (attack at C‐3) have to be revised (5, 13, 17, 18b). In general, electron‐withdrawing substituents at C‐4 fav