Exploiting the Electrophilic and Nucleophilic Dual Role of Nitrile Imines: One-Pot, Three-Component Synthesis of Furo[2,3-d]pyridazin-4(5H)-ones

2015 ◽  
Vol 17 (16) ◽  
pp. 3964-3967 ◽  
Author(s):  
Mariateresa Giustiniano ◽  
Valentina Mercalli ◽  
Jussara Amato ◽  
Ettore Novellino ◽  
Gian Cesare Tron
Keyword(s):  
One Pot ◽  
ChemInform ◽  
2016 ◽  
Vol 47 (1) ◽  
Author(s):  
Mariateresa Giustiniano ◽  
Valentina Mercalli ◽  
Jussara Amato ◽  
Ettore Novellino ◽  
Gian Cesare Tron
Keyword(s):  
One Pot ◽  

2018 ◽  
Vol 54 (65) ◽  
pp. 8960-8963 ◽  
Author(s):  
Xingxing Ma ◽  
Shaoyu Mai ◽  
Yao Zhou ◽  
Gui-Juan Cheng ◽  
Qiuling Song

An efficient one-pot cascade process via unprecedented quadruple cleavage of BrCF2COOEt with primary amines to afford valuable fluorine-containing heterocycles is described, in which BrCF2COOEt plays a dual role as a C1 synthon and a difluoroalkylating reagent for the first time.


2020 ◽  
Vol 16 ◽  
pp. 1447-1455 ◽  
Author(s):  
Gui-Feng Kang ◽  
Gang Zhang

A catalyst-free one-pot synthetic methodology was developed for the preparation of 1,3,5-triazine-2,4-dithione derivatives through three-component reactions of arylaldehydes, thiourea, and orthoformates. The procedure tolerated a diverse range of arylaldehydes and orthoformates and provided a rapid entry to a variety of 4-aryl-6-(alkylthio)-3,4-dihydro-1,3,5-triazine-2(1H)-thiones (29 examples). The synthetic strategy relies on the dual role of thiourea in the cyclization with the aldehydes and the alkylation via an intermediate imidate formation. The structures of 1,3,5-triazine-2,4-dithione derivatives were characterized by spectroscopic techniques as well as by single crystal X-ray diffraction.


RSC Advances ◽  
2016 ◽  
Vol 6 (19) ◽  
pp. 15884-15894 ◽  
Author(s):  
Hunsur Nagendra Nagesh ◽  
Amaroju Suresh ◽  
Muthyala Nagarjuna Reddy ◽  
Narva Suresh ◽  
Jayanty Subbalakshmi ◽  
...  

One-pot synthesis of 1,2,3-triazole tethered benzimidazo[1,2-a]quinolines through a multi-component reaction is demonstrated. Overall one C–C bond and three C–N bonds are formed in a single step.


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