Sodium sulphide promoted synthesis of fused quinoline at room temperature

Author(s):  
Rashmi Singh ◽  
Vishal Prasad Sharma ◽  
Priyanka Yadav ◽  
Priyanka Sonker ◽  
Radhey Mohan Singh ◽  
...  

A novel, simple and eco-friendly strategy for the synthesis of thiopyrano[4,3-b]quinolin-1-ones and pyrrolo[3,4-b]quinolin-1-ones from 2-alkynylquinoline-3-carbonitriles and sodium sulphide (Na2S·9H2O) under catalyst-free conditions at RT.

2021 ◽  
Author(s):  
Wenjing Li ◽  
Shun Li ◽  
Lihua Luo ◽  
Yichen Ge ◽  
Jiaqi Xu ◽  
...  

The catalyst-free oxidative cleavage of (Z)-triaryl-substituted alkenes bearing pyridyl motif with ambient air under irradiation of blue LED at room temperature has been developed. The reaction was facile and scalable,...


2021 ◽  
Vol 58 (5) ◽  
pp. 1179-1191
Author(s):  
Jinpeng Zhang ◽  
Jing Liu ◽  
Lei Dai ◽  
Yuqian Ge ◽  
Linlin Xu ◽  
...  

ChemInform ◽  
2008 ◽  
Vol 39 (47) ◽  
Author(s):  
Janhavi J. Shrikhande ◽  
Manoj B. Gawande ◽  
Radha V. Jayaram

Synlett ◽  
2017 ◽  
Vol 28 (19) ◽  
pp. 2619-2623 ◽  
Author(s):  
Yunxia Wang ◽  
Na Cui ◽  
Yu Zhao

A catalyst-free oxidative [3+2] cycloaddition of phenols and styrenes was developed with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone as the oxidant and 1,1,1,3,3,3-hexafluoropropan-2-ol as the solvent at room temperature. With this method, a broad range of dihydrobenzofurans were efficiently and quickly obtained from readily available phenols and styrenes.


2019 ◽  
Vol 21 (7) ◽  
pp. 1735-1742 ◽  
Author(s):  
Vinayak Botla ◽  
NavyaSree Pilli ◽  
Chandrasekharam Malapaka

Oxygenative cleavage of an inert CAr–NH2 bond with concomitant 1,2 amine migration in 8-aminoquinoline derivatives is achieved through an efficient, catalyst free, one step synthesis of 8-benzyloxy, 7-aminoquinoline directly from 8-aminoquinoline in water at room temperature.


2016 ◽  
Vol 7 (11) ◽  
pp. 2105-2111 ◽  
Author(s):  
Alexander Yuen ◽  
Amaury Bossion ◽  
Enrique Gómez-Bengoa ◽  
Fernando Ruipérez ◽  
Mehmet Isik ◽  
...  

Non-isocyanate polyurethanes (NIPUs) were prepared via polyaddition of highly reactive 8-membered ‘bis-cyclic’ carbonates and various diamines under catalyst-free and room temperature conditions.


2019 ◽  
Vol 31 (11) ◽  
pp. 2532-2536
Author(s):  
Subrahmanya Ishwar Bhat

An expeditious and environmental friendly, general protocol has been developed for the synthesis of 2-amino-3-cyano-4H-chromenes via cascade Knoevenagel-Michael-intramolecular cyclization in water. Pure solid products were obtained by simple filtration technique. The aqueous catalyst-free reactions lead to high product yield at room temperature.


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