Triethyl benzyl ammonium chloride (TEBAC) catalyzed solvent-free one-pot synthesis of pyrimido[4,5-d]pyrimidines

2013 ◽  
Vol 41 (5) ◽  
pp. 2985-2990 ◽  
Author(s):  
Akbar Mobinikhaledi ◽  
Tahere Mosleh ◽  
Naser Foroughifar
Keyword(s):  
Ammonium Chloride ◽  
Solvent Free ◽  
One Pot ◽  
Benzyl Ammonium Chloride ◽  
One Pot Synthesis ◽  
Benzyl Ammonium

ChemInform Abstract: Ammonium Chloride-Catalyzed One-Pot Synthesis of Tetrahydrobenzo[α]xanthen-11-one Derivatives under Solvent-Free Conditions.

ChemInform ◽  
2012 ◽  
Vol 43 (28) ◽  
pp. no-no
Author(s):  
Naser Foroughifar ◽  
Akbar Mobinikhaledi ◽  
Hassan Moghanian ◽  
Reza Mozafari ◽  
Hamid R. M. Esfahani
Keyword(s):  
Ammonium Chloride ◽  
Solvent Free ◽  
One Pot ◽  
One Pot Synthesis ◽  
Solvent Free Conditions

Ammonium chloride catalyzed one-pot synthesis of diindolylmethanes under solvent-free conditions

2007 ◽  
Vol 8 (7) ◽  
pp. 1117-1121 ◽  
Author(s):  
Javad Azizian ◽  
Fatemeh Teimouri ◽  
Mohammad Reza Mohammadizadeh
Keyword(s):  
Ammonium Chloride ◽  
Solvent Free ◽  
One Pot ◽  
One Pot Synthesis ◽  
Solvent Free Conditions

Ammonium Chloride–Catalyzed One-Pot Synthesis of Tetrahydrobenzo[α]xanthen-11-one Derivatives Under Solvent-Free Conditions

2011 ◽  
Vol 41 (18) ◽  
pp. 2663-2673 ◽  
Author(s):  
Naser Foroughifar ◽  
Akbar Mobinikhaledi ◽  
Hassan Moghanian ◽  
Reza Mozafari ◽  
Hamid R. M. Esfahani
Keyword(s):  
Ammonium Chloride ◽  
Solvent Free ◽  
One Pot ◽  
One Pot Synthesis ◽  
Solvent Free Conditions

scholarly journals Tandem Fries Reaction–Conjugate Addition under Microwave Irradiation in Dry Media; One-pot Synthesis of Flavanones

1999 ◽  
Vol 23 (9) ◽  
pp. 574-575
Author(s):  
Firouz Matloubi Moghaddam ◽  
Mohammad Ghaffarzadeh ◽  
Seyed Hossein Abdi-Oskoui
Keyword(s):  
Microwave Irradiation ◽  
Silica Gel ◽  
Conjugate Addition ◽  
Solvent Free ◽  
Naphthalene Derivatives ◽  
One Pot ◽  
Fries Rearrangement ◽  
One Pot Synthesis ◽  
Solvent Free Conditions ◽  
Fries Reaction

An AICl3–ZnCl2 mixture supported on silica gel is found to be an efficient medium for the Fries rearrangement of acyloxybenzene or naphthalene derivatives in solvent-free conditions under microwave irradiation.

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