Iodine(iii) promoted ring-rearrangement reaction of 1-arylamino-2-oxocyclopentane-1-carbonitriles to synthesize N-aryl-δ-valerolactams

2020 ◽  
Vol 18 (4) ◽  
pp. 745-749 ◽  
Author(s):  
Dhananjay Bhattacherjee ◽  
Shaifali ◽  
Ajay Kumar ◽  
Ajay Sharma ◽  
Rituraj Purohit ◽  
...  

Environmentally benign hypervalent iodine(iii) has been utilised selectively for carbocyclic to heterocyclic ring transformation under various electronic conditions with detailed structural and mechanistic investigation.

2020 ◽  
Vol 18 (6) ◽  
pp. 1117-1129 ◽  
Author(s):  
Amritpal Kaur ◽  
Alireza Ariafard

Density functional theory (DFT) at the SMD/M06-2X/def2-TZVP//SMD/M06-2X/LANL2DZ(d),6-31G(d) level was used to explore the regioselective double oxidation of phenols by a hypervalent iodine(v) reagent (IBX) to give o-quinones.


ACS Catalysis ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 6510-6521 ◽  
Author(s):  
Kaveh Farshadfar ◽  
Antony Chipman ◽  
Brian F. Yates ◽  
Alireza Ariafard

2000 ◽  
Vol 55 (6) ◽  
pp. 546-552 ◽  
Author(s):  
A. S. Shaw ◽  
M. A. Abdallah ◽  
M. E. M. Zayed

The synthesis and antimicrobial activity of a series of the title thiones were examined. Reaction of such thiones with hydrazonoyl halides, resulted in ring transformation to give 5-acylhydrazono derivatives of 1,3,4-thiadiazoles. The mechanisms of the studied reactions are discussed.


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