scholarly journals Convenient multicomponent one‐pot synthesis of 2‐iminothiazolines and 2‐aminothiazoles using elemental sulfur under aqueous conditions

Author(s):  
András Gy. Németh ◽  
Bence Marlok ◽  
Attila Domján ◽  
Qinghe Gao ◽  
Xinya Han ◽  
...  
Synlett ◽  
2018 ◽  
Vol 29 (20) ◽  
pp. 2693-2696 ◽  
Author(s):  
Fuhong Xiao ◽  
Guo-Jun Deng ◽  
Shanshan Yuan ◽  
Huawen Huang

An ethylenediamine-promoted three-component synthesis of 3-(thiomethyl)indoles from indoles, thiophenols, and paraformaldehyde has been developed. Water is used as the green solvent in a simple and environmentally friendly procedure. Stable and low-toxicity paraformaldehyde is used as a carbon source.


2019 ◽  
Vol 4 (28) ◽  
pp. 8283-8285
Author(s):  
Zhenzhen Zhan ◽  
Nan Luo ◽  
Haojie Ma ◽  
Jianping He ◽  
Guoqiang Lu ◽  
...  

2020 ◽  
Vol 16 ◽  
pp. 1740-1753 ◽  
Author(s):  
Dharmender Singh ◽  
Vipin Kumar ◽  
Virender Singh

A robust transition-metal-free strategy is presented to access novel β-carboline-tethered benzothiophenone derivatives from 1(3)-formyl-β-carbolines using elemental sulfur activated by Et3N/DMSO. This expeditious catalyst-free reaction proceeds through the formation of β-carboline-based 2-nitrochalcones followed by an incorporation of sulfur to generate multifunctional β-carboline-linked benzothiophenones in good to excellent yields. The synthetic strategy could also be extended towards the synthesis of β-carboline-linked benzothiophenes. Moreover, the afforded products emerged as promising fluorophores and displayed excellent light-emitting properties with quantum yields (ΦF) up to 47%.


1983 ◽  
Vol 12 (4) ◽  
pp. 535-538 ◽  
Author(s):  
Ryu Sato ◽  
Shuji Chiba ◽  
Yuji Takikawa ◽  
Saburo Takizawa ◽  
Minoru Saito

2014 ◽  
Vol 5 (11) ◽  
pp. 3617 ◽  
Author(s):  
Eui Tae Kim ◽  
Woo Jin Chung ◽  
Jaehoon Lim ◽  
Patrick Johe ◽  
Richard S. Glass ◽  
...  

2019 ◽  
Vol 84 (24) ◽  
pp. 16262-16267 ◽  
Author(s):  
Zan Yang ◽  
Yemei Liang ◽  
An Li ◽  
Kun Liu ◽  
Lijun Li ◽  
...  

2016 ◽  
Vol 54 (1) ◽  
pp. 753-757 ◽  
Author(s):  
Maria A. Vodolazhenko ◽  
Anastasiia E. Mykhailenko ◽  
Nikolay Yu. Gorobets ◽  
Sergey M. Desenko

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