Facile Synthesis of [1,2,3]Triazolo[5,1-a]isoquinolines through a Copper-Catalyzed Tandem Sonogashira Coupling/Cyclization Reaction

2016 ◽  
Vol 2016 (33) ◽  
pp. 5470-5473 ◽  
Author(s):  
Mingzhu Fan ◽  
Yi Liu ◽  
Qinquan Hu ◽  
Lihui Jia ◽  
Yunfeng Chen

2018 ◽  
Vol 42 (21) ◽  
pp. 17533-17537
Author(s):  
Sorour Ramezanpour ◽  
Mohammad Nasim Rezaei ◽  
Aref Vaezghaemi ◽  
Frank Rominger

An innovative strategy for synthesis of a library of complex multi-substituted 1,2,4-triazine-6-ones. These structures are analogues of pyrimidine bases with possible enhanced biological activities.





Synlett ◽  
2019 ◽  
Vol 30 (09) ◽  
pp. 1053-1056 ◽  
Author(s):  
Jun Xiong ◽  
Qing Min ◽  
Gang Yao ◽  
Jia-An Zhang ◽  
Hai-Feng Yu ◽  
...  

A new facile synthesis of 3,4-dihydroquinazoline-2(1H)-thiones by an Ugi-azide/Staudinger/aza-Wittig/cyclization sequence has been developed. The Ugi-azide reactions of 2-azidobenzaldehydes, amines, trimethylsilyl azide, and isocyanides produced tetrazoles, which, when treated with methyldiphenylphosphane and CS2, produced 3,4-dihydroquinazoline-2(1H)-thiones in good overall yields via a sequential Staudinger/aza-Wittig/cyclization reaction.





2018 ◽  
Vol 16 (21) ◽  
pp. 4013-4020 ◽  
Author(s):  
Akinari Sumita ◽  
Jinhee Lee ◽  
Yuko Otani ◽  
Tomohiko Ohwada

We present a one-pot two-step methodology, in which an unprotected amino is tolerated, for rapidly synthesizing 2,3-benzodiazepines via phosphate-assisted acylation reaction and hydrazine cyclization reaction.







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