1-Indanones have been successfully prepared by means of three different non-conventional techniques, namely microwaves, high-intensity ultrasound and a Q-tube™ reactor. A library of differently substituted 1-indanones has been prepared via one-pot intramolecular Friedel-Crafts acylation and their efficiency and “greenness” have been compared
The indan ring system is present in several compounds with important pharmacological properties. In ...
AbstractA one-pot protocol based on coupling-cyclization strategy has been developed for the constru...
A new and efficient protocol to prepare indenes is reported. Assisted by boron trifluoride diethyl e...
A series of 1-indanones were synthesized in good yields via tandem Friedel-Crafts acylation and Naza...
In medicinal chemistry, there is a constant need for new preparative methods, both to make the synth...
In medicinal chemistry, there is a constant need for new preparative methods, both to make the synth...
One-pot synthetic processes are considered as convenient methods to synthesize organic molecules wit...
The intramolecular Friedel-Crafts acylation reaction of 3-arylpropanoic acids to give 1-indanones ca...
Superacid promoted intramolecular acylation of simple cinnamic acid esters for the synthesis of inde...
<p>A novel, efficient and convenient procedure has been developed for the synthesis of 2-(4-amino-su...
The synthesis of the pyrazino[1,2-α]indole nucleus was achieved by intramolecular cyclization of sev...
The indan ring system is present in several compounds with important pharmacological properties. In ...
We report a facile and highly efficient method that copper-catalyzed intramolecular annulation to sy...
A facile, superacid-promoted, domino, one-pot synthesis of novel spirotetracyclic indanones through ...
The solvent-free indium-promoted reaction of alkanoyl chlorides with sterically and electronically d...
The indan ring system is present in several compounds with important pharmacological properties. In ...
AbstractA one-pot protocol based on coupling-cyclization strategy has been developed for the constru...
A new and efficient protocol to prepare indenes is reported. Assisted by boron trifluoride diethyl e...
A series of 1-indanones were synthesized in good yields via tandem Friedel-Crafts acylation and Naza...
In medicinal chemistry, there is a constant need for new preparative methods, both to make the synth...
In medicinal chemistry, there is a constant need for new preparative methods, both to make the synth...
One-pot synthetic processes are considered as convenient methods to synthesize organic molecules wit...
The intramolecular Friedel-Crafts acylation reaction of 3-arylpropanoic acids to give 1-indanones ca...
Superacid promoted intramolecular acylation of simple cinnamic acid esters for the synthesis of inde...
<p>A novel, efficient and convenient procedure has been developed for the synthesis of 2-(4-amino-su...
The synthesis of the pyrazino[1,2-α]indole nucleus was achieved by intramolecular cyclization of sev...
The indan ring system is present in several compounds with important pharmacological properties. In ...
We report a facile and highly efficient method that copper-catalyzed intramolecular annulation to sy...
A facile, superacid-promoted, domino, one-pot synthesis of novel spirotetracyclic indanones through ...
The solvent-free indium-promoted reaction of alkanoyl chlorides with sterically and electronically d...
The indan ring system is present in several compounds with important pharmacological properties. In ...
AbstractA one-pot protocol based on coupling-cyclization strategy has been developed for the constru...
A new and efficient protocol to prepare indenes is reported. Assisted by boron trifluoride diethyl e...
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