1293294-69-5

Upstream product

• 504440-54-4 2-[3-(trimethylsilyl)prop-2-ynylthio]benzo[d]thiazole 
• 2492-26-4 sodium 2-mercaptobenzothiazole 
• 27126-20-1 (3-azidopropyl)benzene 
• 1293294-61-7 2-[1-fluoro-3-(trimethylsilyl)prop-2-ynylsulfonyl]benzo[d]thiazole 

Downstream Products

• 1293294-96-8 (Z)-4-(3-ethyl-1-fluoropent-1-en-1-yl)-1-(3-phenylpropyl)-1H-1,2,3-triazole 
• 1293294-87-7 (Z)-4-(1-fluoro-2-mesitylvinyl)-1-(3-phenylpropyl)-1H-1,2,3-triazole 
• 1293295-00-7 (Z)-4-(1-fluoronon-1-en-1-yl)-1-(3-phenylpropyl)-1H-1,2,3-triazole 
• 1293294-92-4 (Z)-4-[1-fluoro-2-(4-nitrophenyl)vinyl]-1-(3-phenylpropyl)-1H-1,2,3-triazole 
• 1293294-90-2 (Z)-4-[1-fluoro-2-(4-methoxyphenyl)vinyl]-1-(3-phenylpropyl)-1H-1,2,3-triazole 

Relevant academic research and scientific papers

E- or Z-Selective synthesis of 4-fluorovinyl-1,2,3-triazoles with fluorinated second-generation Julia-Kocienski reagents

A highly modular approach to N-substituted 4-(1-fluorovinyl)triazoles is described. In situ desilylation and Cu-catalyzed ligation reaction of TMS-protected α-fluoropropargyl benzothiazole sulfone with aryl, alkyl, and metallocenyl azides furnished second

Facile synthesis of 4-vinyl- and 4-fluorovinyl-1,2,3-triazoles via bifunctional "click-olefination" reagents

Modular synthesis of vinyl and fluorovinyl triazoles can be achieved from bifunctional propargyl and fluoropropargyl sulfones by Cu-catalyzed azide-alkyne ligation and Julia-Kocienski olefination. Competitive click reactions of the protio and fluoropropar