Efficient and rapid synthesis of N-substituted isoquinolin-1-ones under mild conditions: Facile access to doryanine derivatives
-
Add time:09/01/2019 Source:sciencedirect.com
We describe the simple and efficient synthesis of N-substituted isoquinolin-1-one derivatives. Initiating with the coupling of benzoic acids containing vinyl ethers with different amines, followed by rapid intramolecular cyclization under acidic conditions at room temperature, N-substituted isoquinolin-1-ones were furnished in high yields. The utility of this simple and mild cyclization method was demonstrated through the practical synthesis of natural product doryanine and its analogues.
We also recommend Trading Suppliers and Manufacturers of N-(2-bromo-4-methylphenyl)-4-methoxybenzamide (cas 111270-65-6). Pls Click Website Link as below: cas 111270-65-6 suppliers
Prev:Copper-catalyzed denitrogenative N-arylation of sulfoximines and sulfonamides with arylhydrazines
Next:Translational ToolboxPhase II Trials in Drug Development and Adaptive Trial Design) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Copper-catalyzed denitrogenative N-arylation of sulfoximines and sulfonamides with arylhydrazines08/31/2019
- Original ArticleBiological investigation of novel metal complexes of 2-amino-4-substituted phenylthiazole Schiff bases08/30/2019
- Crystal structure, spectroscopic investigations and quantum chemical calculation studies of (3aR,6S,7aR)-7a-bromo-6-methyl-2-[(4-methylphenyl)sulfonyl]-1,2,3,6,7,7a-hexahydro-3a,6-epoxyisoindole: A combined experimental and theoretical studies08/29/2019


