Regioselective Synthesis, Spectroscopic Characterization, and Computational Chemical Study of Spiro[Indoline-3,4’-Pyrazolo[3,4-b] Pyridine Derivatives as Agrochemical Agents

Author(s):  
Nasser Abdelmoneim Ibrahim ◽  
Sarah Ahmed El-Kaed ◽  
Sameh Ahmed Rizk ◽  
Ali Khalil Ali
2019 ◽  
Vol 17 (3) ◽  
pp. 646-654 ◽  
Author(s):  
Luis A. López ◽  
Javier González

This work reports a computational study of the copper(i)-catalyzed regioselective synthesis of indolizine derivatives through the [3 + 2]-cyclization reaction of vinyldiazo acetates and pyridine derivatives.


Synlett ◽  
2010 ◽  
Vol 2011 (01) ◽  
pp. 116-120 ◽  
Author(s):  
K. Majumdar ◽  
Raj Nandi ◽  
Sintu Ganai ◽  
Abu Taher

2004 ◽  
Vol 45 (21) ◽  
pp. 4031-4034 ◽  
Author(s):  
Francisco Palacios ◽  
Concepción Alonso ◽  
Gloria Rubiales ◽  
Maite Villegas

2010 ◽  
Vol 51 (33) ◽  
pp. 4350-4353 ◽  
Author(s):  
Kurissery A. Tony ◽  
Santhosh Kumar Chittimalla ◽  
G. Abraham Rajkumar ◽  
Anjan Chakrabarti

2013 ◽  
Vol 31 (7) ◽  
pp. 950-954 ◽  
Author(s):  
Yindi Yang ◽  
Min Zhang ◽  
Yiwen Zhu ◽  
Li Zhang ◽  
Qiqiang Xie ◽  
...  

Synthesis ◽  
2019 ◽  
Vol 51 (19) ◽  
pp. 3600-3610 ◽  
Author(s):  
Tumula Nagaraju ◽  
Palakodety Radha Krishna ◽  
Balasubramanian Sridhar ◽  
Nakka Mangarao

An effective and expeditious approach for the construction of biologically important 5-guanidino-1,2,4-thiadiazole and 1,2,4-triazolo[1,5-a]pyridine derivatives has been developed. This new protocol involves the phenyliodine(III) diacetate [PhI(OAc)2]-mediated oxidative cyclization of thioureas/2-aminopyridines and imidates via N–S and N–N bond formation at ambient temperature. This method furnishes the versatile 5-guanidino-1,2,4-thiadiazoles and 1,2,4-triazolo[1,5-a]pyridines in a scalable manner with high efficiency and excellent regioselectivity.


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