A metal-free tandem approach to prepare structurally diverse N-heterocycles: synthesis of 1,2,4-oxadiazoles and pyrimidinones

2014 ◽  
Vol 38 (7) ◽  
pp. 3062-3070 ◽  
Author(s):  
Puneet K. Gupta ◽  
Mohd. Kamil Hussain ◽  
Mohd. Asad ◽  
Ruchir Kant ◽  
Rohit Mahar ◽  
...  
Keyword(s):  
One Pot ◽  

N-heterocycles, namely 1,2,4-oxadiazoles and 2,6 disubstituted pyrimidin-4-ones, have been synthesised in one pot via carboxamidation of amidines with aryl carboxylic acids and aryl propargylic acids under metal-free conditions.

2020 ◽  
Vol 56 (20) ◽  
pp. 3073-3076 ◽  
Author(s):  
Francesca Franco ◽  
Sara Meninno ◽  
Maurizio Benaglia ◽  
Alessandra Lattanzi

A direct and general one-pot approach to α-trifluoromethylthiolated amides, esters and carboxylic acids has been successfully developed under mild, catalytic and metal-free conditions.


Synthesis ◽  
2013 ◽  
Vol 46 (03) ◽  
pp. 320-330 ◽  
Author(s):  
Danfeng Huang ◽  
Yulai Hu ◽  
Teng Niu ◽  
Ke-Hu Wang ◽  
Changming Xu ◽  
...  

ChemInform ◽  
2006 ◽  
Vol 37 (7) ◽  
Author(s):  
Santosh Rudrawar ◽  
Atul Kondaskar ◽  
Asit K. Chakraborti

ChemInform ◽  
2014 ◽  
Vol 45 (29) ◽  
pp. no-no
Author(s):  
Teng Niu ◽  
Ke-Hu Wang ◽  
Danfeng Huang ◽  
Changming Xu ◽  
Yingpeng Su ◽  
...  

Synthesis ◽  
2005 ◽  
Vol 2005 (15) ◽  
pp. 2521-2526 ◽  
Author(s):  
Asit Chakraborti ◽  
Santosh Rudrawar ◽  
Atul Kondaskar

Synlett ◽  
2018 ◽  
Vol 29 (11) ◽  
pp. 1505-1509 ◽  
Author(s):  
Meichao Li ◽  
Zhenlu Shen ◽  
Liang Xu ◽  
Shengpeng Wang ◽  
Bajin Chen ◽  
...  

A metal-free and one-pot two-step synthesis of aryl carboxylic acids from aryl alkyl ketones has been achieved. The reactions were performed with iodine as the catalyst, DMSO and TBHP as the oxidants. Under the optimal reaction conditions, a number of aryl alkyl ketones could be converted into their corresponding aryl carboxylic acids in good to excellent yields (up to 94%).


SynOpen ◽  
2021 ◽  
Author(s):  
Vinod K Tiwari ◽  
MANGAL SINGH YADAV ◽  
Manoj K Jaiswal ◽  
Sunil Kumar

A facile route for the synthesis of diverse range of N-acylbenzotriazole derivatives from corresponding carboxylic acids has been established through carbonyl activation pathway. In this method, trichloroacetonitrile is performed as an effective reagent for an easy access of N-acylbenzotriazoles which was simply proceed through the activation of carboxylic acids via in situ imidate formation in anhydrous 1,2 dichloroethane followed by addition of 1H-benzotriazole at 80 oC for 3-4 hours. Easy handling, one-pot, and metal-free condition demonstrate the notable merits of the devised protocol.


2018 ◽  
Vol 21 (28) ◽  
Author(s):  
Yan Fang Sun ◽  
Guo He Xu ◽  
Min Jie Gao ◽  
Qiu Ling Hu ◽  
Jing Jun Ma
Keyword(s):  
One Pot ◽  

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