𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Electrochemically Induced N-Alkylation of Pyrroles.

✍ Scribed by Marta Feroci; Achille Inesi; Leucio Rossi; Giancarlo Sleiter

Publisher
John Wiley and Sons
Year
2010
Weight
33 KB
Volume
30
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Electrochemically Induced N-Alkylation o
Electrochemically Induced N-Alkylation of Pyrroles
✍ Marta Feroci; Achille Inesi; Leucio Rossi; Giancarlo Sleiter πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 198 KB

Electrochemically generated tetraethylammonium peroxy-corresponding N-alkylated pyrroles in high yields. C-Alkylated pyrroles have not been isolated in any case dicarbonate (TEAPC) and tetraethylammonium carbonate (TEAC) react under very mild conditions with pyrroles reported. affording, after addit

Reductive N Alkylation of Cyclo[8]pyrrol
Reductive N Alkylation of Cyclo[8]pyrroles
✍ Thomas KΓΆhler; Zhongping Ou; Jeong Tae Lee; Daniel Seidel; Vincent Lynch; Karl M πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 201 KB

## Cyclo[8] pyrrole (1), although lacking bridging meso carbon atoms, may be considered as a larger analogue of porphyrin (2) in that it is flat and aromatic (see Scheme 1). [1] For this reason, we have been interested in exploring the chemical behavior of cyclo [8]pyrrole and contrasting it to th