Background: Phthalides are privileged constituents of numerous pharmaceuticals, natural products and agrochemicals and exhibit several biological and therapeutic activities. Therefore, the development of new, facile, and sustainable strategies for the construction of these moieties is highly desired.Results: A broad substrate scope for β-keto acids was found to be strongly compatible with this catalytic process, affording a wide variety of 3-substituted phthalides in good to excellent yields.Conclusion: A concise and efficient synthesis strategy of 3-substituted phthalides from 2-formylbenzoic acid and β-keto acids via a catalytic one-pot cascade reaction in glycerol has been accomplished
3-Alkylidenephtalides represent a large class of structurally diverse molecules containing natural p...
710-712Use of the modified reagent system of NaBH₄-Amberlyst-15 (H⁺) for the reduction of o-aroylben...
3-Alkylidenephtalides represent a large class of structurally diverse molecules containing natural p...
International audienceAn efficient organophotocatalyzed protocol was developed for the preparation o...
In recent years development of environmentally friendly chemical synthesis is gaining considerable i...
In recent years development of environmentally friendly chemical synthesis is gaining considerable i...
In recent years development of environmentally friendly chemical synthesis is gaining considerable i...
In recent years development of environmentally friendly chemical synthesis is gaining considerable i...
The surprisingly facile conversion (isomerization) of 2-formyl-arylketones into 3-substituted phthal...
Natural products have been a source of inspiration for chemists and chemical biologists for many yea...
3-Alkylidenephtalides represent a large class of structurally diverse molecules containing natural p...
3-Alkylidenephtalides represent a large class of structurally diverse molecules containing natural p...
3-Alkylidenephtalides represent a large class of structurally diverse molecules containing natural p...
3-Alkylidenephtalides represent a large class of structurally diverse molecules containing natural p...
In this thesis, we demonstrated the new reaction mode enabled by NHC in the enantiose...
3-Alkylidenephtalides represent a large class of structurally diverse molecules containing natural p...
710-712Use of the modified reagent system of NaBH₄-Amberlyst-15 (H⁺) for the reduction of o-aroylben...
3-Alkylidenephtalides represent a large class of structurally diverse molecules containing natural p...
International audienceAn efficient organophotocatalyzed protocol was developed for the preparation o...
In recent years development of environmentally friendly chemical synthesis is gaining considerable i...
In recent years development of environmentally friendly chemical synthesis is gaining considerable i...
In recent years development of environmentally friendly chemical synthesis is gaining considerable i...
In recent years development of environmentally friendly chemical synthesis is gaining considerable i...
The surprisingly facile conversion (isomerization) of 2-formyl-arylketones into 3-substituted phthal...
Natural products have been a source of inspiration for chemists and chemical biologists for many yea...
3-Alkylidenephtalides represent a large class of structurally diverse molecules containing natural p...
3-Alkylidenephtalides represent a large class of structurally diverse molecules containing natural p...
3-Alkylidenephtalides represent a large class of structurally diverse molecules containing natural p...
3-Alkylidenephtalides represent a large class of structurally diverse molecules containing natural p...
In this thesis, we demonstrated the new reaction mode enabled by NHC in the enantiose...
3-Alkylidenephtalides represent a large class of structurally diverse molecules containing natural p...
710-712Use of the modified reagent system of NaBH₄-Amberlyst-15 (H⁺) for the reduction of o-aroylben...
3-Alkylidenephtalides represent a large class of structurally diverse molecules containing natural p...