Solvent-Free One-Pot Reduction of Imines Generated in situ from Aldehydes and Aniline by Tributyltin Hydride on Silica Gel

2002 ◽  
Vol 31 (3) ◽  
pp. 274-275 ◽  
Author(s):  
Ryoichi Hiroi ◽  
Norikazu Miyoshi ◽  
Makoto Wada
1999 ◽  
Vol 23 (9) ◽  
pp. 574-575
Author(s):  
Firouz Matloubi Moghaddam ◽  
Mohammad Ghaffarzadeh ◽  
Seyed Hossein Abdi-Oskoui

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.


ChemInform ◽  
2010 ◽  
Vol 41 (44) ◽  
pp. no-no
Author(s):  
Gowravaram Sabitha ◽  
N. Mallikarjuna Reddy ◽  
M. Nagendra Prasad ◽  
G. S. K. Raja ◽  
J. S. Yadav

2014 ◽  
Vol 10 ◽  
pp. 26-33 ◽  
Author(s):  
Samir Kundu ◽  
Babli Roy ◽  
Basudeb Basu

The development of a silica-promoted highly selective synthesis of 1,2 or 1,3-dithioethers via solvent-free one-pot tandem reactions of an allyl bromide with excess thiol at room temperature is described. The choice of silica gel, either pre-calcined or moistened with water, exhibited notable regioselectivity in the formation of dithioethers. Plausible mechanistic routes were explored and postulated.


AIChE Journal ◽  
2018 ◽  
Vol 64 (11) ◽  
pp. 4027-4038 ◽  
Author(s):  
Hui Sun ◽  
Zhongwei Sun ◽  
Benxian Shen ◽  
Jichang Liu ◽  
Gengnan Li ◽  
...  

2015 ◽  
Vol 93 (11) ◽  
pp. 1245-1248 ◽  
Author(s):  
Ahmad Reza Moosavi-Zare ◽  
Mohammad Ali Zolfigol ◽  
Fateme Derakhshan-Panah ◽  
Masoume Daraei

A one-pot, multicomponent condensation reaction of phenols, aromatic aldehydes, and amides in the presence of catalytic amount of trityl chloride as a homogeneous organocatalyst under solvent-free condition to prepare amidoalkyl phenols has been reported. It is interesting that trityl chloride by in situ generation of trityl carbocation with inherent instability catalyzes the reaction.


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