scholarly journals Post-Ugi gold-catalyzed diastereoselective domino cyclization for the synthesis of diversely substituted spiroindolines

2013 ◽  
Vol 9 ◽  
pp. 2097-2102 ◽  
Author(s):  
Amit Kumar ◽  
Dipak D Vachhani ◽  
Sachin G Modha ◽  
Sunil K Sharma ◽  
Virinder S Parmar ◽  
...  

An Ugi four-component reaction of propargylamine with 3-formylindole and various acids and isonitriles produces adducts which are subjected to a cationic gold-catalyzed diastereoselective domino cyclization to furnish diversely substituted spiroindolines. All the reactions run via an exo-dig attack in the hydroarylation step followed by an intramolecular diastereoselective trapping of the imminium ion. The whole sequence is atom economic and the application of a multicomponent reaction assures diversity.

2008 ◽  
Vol 2 (2) ◽  
pp. 152-156 ◽  
Author(s):  
Guoping Chen ◽  
Michiaki Takezawa ◽  
Naoki Kawazoe ◽  
Tetsuya Tateishi

2021 ◽  
Author(s):  
Yan Wu ◽  
Jin-Yang Chen ◽  
Jing Ning ◽  
Xue Jiang ◽  
Jie Deng ◽  
...  

An electrochemical multicomponent reaction was established under catalyst-, chemical-oxidant-free and mild conditions, which provides an eco-friendly and simple protocol for constructing 4-selanylpyrazoles from easily available raw materials with high yields.


2021 ◽  
Vol 23 (1) ◽  
pp. 329-338
Author(s):  
Ethan M. Cunningham ◽  
Alice E. Green ◽  
Gabriele Meizyte ◽  
Alexander S. Gentleman ◽  
Peter W. Beardsmore ◽  
...  

Infrared multiple-photon dissociation spectroscopy reveals the nature of nitrous oxide binding to metal clusters.


ChemInform ◽  
2012 ◽  
Vol 43 (18) ◽  
pp. no-no
Author(s):  
Li-Jun Geng ◽  
Guo-Liang Feng ◽  
Jiu-Gao Yu ◽  
Hong-Li Zhang ◽  
Yu-Mei Zhang

Author(s):  
Xing‐Yong Zhu ◽  
Chuan‐Kun Ran ◽  
Ming Wen ◽  
Gui‐Ling Guo ◽  
Yuan Liu ◽  
...  

Molecules ◽  
2021 ◽  
Vol 26 (2) ◽  
pp. 303
Author(s):  
András Gy. Németh ◽  
Renáta Szabó ◽  
György Orsy ◽  
István M. Mándity ◽  
György M. Keserű ◽  
...  

We have developed the continuous-flow synthesis of thioureas in a multicomponent reaction starting from isocyanides, amidines, or amines and sulfur. The aqueous polysulfide solution enabled the application of sulfur under homogeneous and mild conditions. The crystallized products were isolated by simple filtration after the removal of the co-solvent, and the sulfur retained in the mother liquid. Presenting a wide range of thioureas synthesized by this procedure confirms the utility of the convenient continuous-flow application of sulfur.


Sign in / Sign up

Export Citation Format

Share Document