Microwave assisted alkylation of ortho-methyl-tetra-C-naphthyl-resorcinarene and its phosphorylated derivatives with haloalkanes and ethyl bromoacetate

2018 ◽  
Vol 59 (26) ◽  
pp. 2586-2589 ◽  
Author(s):  
Olga S. Serkova ◽  
Valentina V. Glushko ◽  
Maria A. Egorova ◽  
Vera I. Maslennikova
2005 ◽  
Vol 2005 (3) ◽  
pp. 167-168 ◽  
Author(s):  
Gui-Rong Qu ◽  
Yong Li ◽  
Su-Hui Han

The synthesis of N1/N9- (Ethoxycarbonylmethyl)pyrimidine/purine using as synthons for peptide nucleic acids has been described. Microwave irradiation provided the desired products by alkylation of the appropriately protected natural and substituted nucleobases with ethyl bromoacetate within 4–7 min in 48–85% yields.


2019 ◽  
Vol 16 (6) ◽  
pp. 495-500
Author(s):  
Asma Mehrez ◽  
Dalila Mtat ◽  
Ridha Touati

An efficient and rapid synthesis of a new class of chiral oxime ethers has been achieved via two-step reaction in which the first step is the reaction of oximes 1a-f with ethyl bromoacetate in the presence of sodium hydride to give oxime ethers 2a-f which are subsequently, in the second step, reacted with different commercially available chiral amines under microwave irradiation conditions to give compounds 3a-l in good to excellent yields. Through this method, we have observed a decrease in reaction time and excellent yields than the previously described conventional method.


Planta Medica ◽  
2009 ◽  
Vol 75 (09) ◽  
Author(s):  
I Stanisavljević ◽  
M Lazić ◽  
N Radulović ◽  
V Veljković

2015 ◽  
Author(s):  
Corinne Fruit ◽  
Julien Godeau ◽  
Marine Harari ◽  
Sylvain Laclef ◽  
Vincent Levacher ◽  
...  

Author(s):  
Marcin Lukasiewicz ◽  
Anna Osowiec ◽  
Magdalena Marciniak

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