Iodine-mediated one-pot synthesis of C-3 acylated indolizines from pyridines, aryl methyl ketones and acrylate derivatives
-
Add time:07/24/2019 Source:sciencedirect.com
An I2/CuI-promoted multi-component reaction from pyridines, aryl methyl ketones and electron deficient acrylates has been accomplished in a “one-pot” manner, which provides a straightforward and efficient access to C-3 acylated indolizines. The key intermediate of N-ylides is hypothesized to be generated in situ from pyridines and (hetero)aryl methyl ketones in the presence of iodine. This method has been applied in the synthesis of two molecules with anticonvulsant and anti-inflammatory activities.
We also recommend Trading Suppliers and Manufacturers of 3-Chloro-2-iodo-5-(trifluoromethyl)pyridine (cas 134161-12-9). Pls Click Website Link as below: cas 134161-12-9 suppliers
Prev:Structural basis for α-bungarotoxin insensitivity of neuronal nicotinic acetylcholine receptors
Next:Fluorinated pyridine derivatives) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Fluorinated pyridine derivatives07/25/2019


