Graphene oxide as an acid catalyst for the room temperature ring opening of epoxides

2012 ◽  
Vol 48 (44) ◽  
pp. 5443 ◽  
Author(s):  
Amarajothi Dhakshinamoorthy ◽  
Mercedes Alvaro ◽  
Patricia Concepción ◽  
Vicente Fornés ◽  
Hermenegildo Garcia
ChemInform ◽  
2012 ◽  
Vol 43 (40) ◽  
pp. no-no
Author(s):  
Amarajothi Dhakshinamoorthy ◽  
Mercedes Alvaro ◽  
Patricia Concepcion ◽  
Vicente Fornes ◽  
Hermenegildo Garcia

2005 ◽  
Vol 83 (5) ◽  
pp. 505-507 ◽  
Author(s):  
Najmodin Azizi ◽  
Mohammad R Saidi

Lithium perchlorate catalyzed the ring opening of epoxides with amines to provide the corresponding β-aminoalcohols in excellent yields with high regioselectivity. The reaction proceeds rapidly under mild and neutral conditions and worked well with primary, secondary, aliphatic, aromatic, and hindered amines in short times at room temperature, in the absence of solvent.Key words: epoxide, lithium perchlorate, β-aminoalcohols, solvent-free.


2007 ◽  
Vol 2 (2) ◽  
pp. 1934578X0700200
Author(s):  
Suchitra Bhatt ◽  
Sandip K. Nayak

Anhydrous titanium(III) chloride was found to be a simple and efficient Lewis acid catalyst for ring opening of epoxides at ambient temperature. The reaction proceeded smoothly with anilines as well as azide ion as nucleophiles to give the corresponding β-amino alcohols and β-azido alcohols in moderate to good yields.


2014 ◽  
Vol 55 (49) ◽  
pp. 6694-6697 ◽  
Author(s):  
Maryam Mirza-Aghayan ◽  
Mahdi Alizadeh ◽  
Mahdieh Molaee Tavana ◽  
Rabah Boukherroub

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