A one-pot synthesis of [1,2,3]triazolo[1,5-a]quinoxalines from 1-azido-2-isocyanoarenes with high bond-forming efficiency

2017 ◽  
Vol 53 (7) ◽  
pp. 1305-1308 ◽  
Author(s):  
Dengke Li ◽  
Tingting Mao ◽  
Jinbo Huang ◽  
Qiang Zhu

An efficient approach to prepare 1,2,3-triazolo[1,5-a]quinoxaline scaffolds, starting from 1-azido-2-isocyanoarenes and terminal acetylenes or substituted acetaldehydes, has been developed.

2020 ◽  
Author(s):  
Lucien Caspers ◽  
Julian Spils ◽  
Mattis Damrath ◽  
Enno Lork ◽  
Boris Nachtsheim

In this article we describe an efficient approach for the synthesis of cyclic diaryliodonium salts. The method is based on benzyl alcohols as starting materials and consists of an Friedel-Crafts-arylation/oxidation sequence. Besides a deep optimization, particluar focusing on the choice and ratios of the utilized Bronsted-acids and oxidants, we explore the substrate scope of this transformation. We also discuss an interesting isomerism of cyclic iodonium salts substituted with aliphatic substituents at the bridge head carbon. <br>


RSC Advances ◽  
2016 ◽  
Vol 6 (70) ◽  
pp. 66320-66323 ◽  
Author(s):  
Xiao-Zhuan Zhang ◽  
Dao-Liang Ge ◽  
Shan-Yong Chen ◽  
Xiao-Qi Yu

A facile and efficient approach to 3-thiocyanato-4H-chromen-4-ones from enaminones and KSCN was realized at room temperature. In addition, one-pot synthesis of 3-thiocyanatochromenones from 2-hydroxylacetophenones was also developed.


2007 ◽  
Vol 48 (12) ◽  
pp. 2097-2099 ◽  
Author(s):  
Kristin Odlo ◽  
Edmund André Høydahl ◽  
Trond Vidar Hansen

ChemInform ◽  
2012 ◽  
Vol 43 (11) ◽  
pp. no-no
Author(s):  
Farzad Nikpour ◽  
Mahnaz Sharafi-Kolkeshvandi ◽  
Asrin Bahmani

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