- Short Note
Aromatic aldehydes react with dimethyl acetonedicarboxylate in molar ratio 1:2 with spontaneous intermolecular Michael addition to give polysubstituted cyclohexanones [1].[...]
2003 May - 12 articles
Aromatic aldehydes react with dimethyl acetonedicarboxylate in molar ratio 1:2 with spontaneous intermolecular Michael addition to give polysubstituted cyclohexanones [1].[...]
Aromatic aldehydes react with dimethyl acetonedicarboxylate in molar ratio 1:2 with spontaneous intramolecular Michael addition to give polysubstituted cyclohexanones [1].[...]
Aromatic aldehydes react with dimethyl acetonedicarboxylate in molar ratio 1:2 with spontaneous intramolecular Michael addition to give polysubstituted cyclohexanones [1].[...]
The discussion and purpose for the synthesis of this compound has been reported elsewhere [1].[...]
The discussion and purpose for the synthesis of this compound has been reported elsewhere [1].[...]
The discussion and purpose for the synthesis of this compound has been reported elsewhere [1].[...]
The discussion and purpose for the synthesis of this compound has been reported elsewhere [1].[...]
The discussion and purpose for the synthesis of this compound has been reported elsewhere [1].[...]
The discussion and purpose for the synthesis of this compound has been reported elsewhere [1].[...]
The discussion and purpose for the synthesis of this compound has been reported elsewhere [1].[...]
As part of ongoing research programme we synthesised the title compounds as valuable intermediates for intramolecular cycloaddition reactions, leading to biologically active heterocycles.[...]
The discussion and purpose for the synthesis of this compound has been reported elsewhere [1].[...]