scholarly journals One-pot, sequential four-component synthesis of novel heterocyclic [3.3.3] propellane derivatives at room temperature

RSC Advances ◽  
2018 ◽  
Vol 8 (26) ◽  
pp. 14171-14176 ◽  
Author(s):  
Maryam Beyrati ◽  
Alireza Hasaninejad

An efficient synthesis of propellane derivatives is described by the condensation reaction between acenaphthenequinone, malono derivatives, primary amines and β-ketoesters or β-diketones in the presence of triethylamine in ethanol at room temperature.

2008 ◽  
Vol 38 (7) ◽  
pp. 1078-1089 ◽  
Author(s):  
Saeed Balalaie ◽  
Sorour Ramezanpour ◽  
Morteza Bararjanian ◽  
Jürgen H. Gross

ChemInform ◽  
2008 ◽  
Vol 39 (38) ◽  
Author(s):  
Saeed Balalaie ◽  
Sorour Ramezanpour ◽  
Morteza Bararjanian ◽  
Juergen H. Gross

Synlett ◽  
2017 ◽  
Vol 28 (17) ◽  
pp. 2295-2298
Author(s):  
Kommula Dileep ◽  
M. Murty

A simple and efficient synthetic protocol has been developed involving a one-pot three-component reaction of a 2-chlorobenzazole, piperazine, and an arenesulfonyl chloride under aqueous conditions at room temperature in the absence of a catalyst, ligand, or base. By using this protocol, a variety of 2-[4-(arylsulfonyl)piperazin-1-yl]-1,3-benzothiazole, -1H-benzimidazole, and -1,3-benzoxazole derivatives were synthesized in excellent yields.


2001 ◽  
Vol 7 (5) ◽  
Author(s):  
Fawi M. Abd El Latif ◽  
Mohamed A. Khalil ◽  
Islam Helmy ◽  
Hausien A Solieman

Synthesis ◽  
2018 ◽  
Vol 51 (02) ◽  
pp. 522-529 ◽  
Author(s):  
Deqing Shi ◽  
Lingna Wang ◽  
Tiancong Ma ◽  
Mingming Qiao ◽  
Qiangxian Wu ◽  
...  

A visible-light photoredox-catalyzed oxidation/[3+2] cycloaddition/oxidative aromatization cascade reaction of [(3,4-dihydroisoquinolin-2(1H)-yl)methyl]phosphonates and activated olefins or alkynes for the efficient synthesis of potentially biological active pyrrolo[2,1-a]isoquinoline-substituted phosphonates was developed. This transformation features mild reaction conditions (i.e., visible light irradiation, room temperature), molecular oxygen (O2) as a green oxidant, simple ‘one-pot’ operation.


2019 ◽  
Vol 15 ◽  
pp. 874-880
Author(s):  
Razieh Navari ◽  
Saeed Balalaie ◽  
Saber Mehrparvar ◽  
Fatemeh Darvish ◽  
Frank Rominger ◽  
...  

An efficient approach for the synthesis of pyrazolopyridines containing the aminochromane motif through a base-catalyzed cyclization reaction is reported. The synthesis was carried out through a three-component reaction of (arylhydrazono)methyl-4H-chromen-4-one, malononitrile, primary amines in the presence of Et3N at room temperature. However, carrying out the reaction under the same conditions without base led to a fused chromanyl-cyanopyridine. High selectivity, high atom economy, and good to high yields in addition to mild reaction conditions are the advantages of this approach.


Synthesis ◽  
2018 ◽  
Vol 50 (11) ◽  
pp. 2191-2199 ◽  
Author(s):  
Yongde Zhao ◽  
Shengqiang Guo ◽  
Yang Zhou ◽  
Bencai Dai ◽  
Cuimeng Huo ◽  
...  

A concise one-pot three-component reaction of organic halides­, terminal acetylenes, and sodium azide provided an efficient route for the synthesis of 1,2,3-triazoles. A variety of 1,2,3-triazoles were prepared in good to excellent yields with green solvent glycerol. This procedure used CuI and diethylamine, which are two easily available reagents as the new catalytic system at room temperature.


2011 ◽  
Vol 64 (12) ◽  
pp. 1624 ◽  
Author(s):  
Shahana A. Chowdhury ◽  
Pamela M. Dean ◽  
R. Vijayaraghavan ◽  
D. R. MacFarlane

A direct, one pot synthesis of an ellagic acid salt was achieved at room temperature by dimerization of ethyl gallate using N,N-dimethylammonium N′,N′-dimethylcarbamate, a distillable ionic liquid, as solvent.


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