127084-56-4

Upstream product

• 127084-48-4 C₂₁H₃₈OSSn 
• 622-08-2 2-Benzyloxyethanol 
• 4981-83-3 2-(Benzyloxy)ethyl p-toluenesulfonate 

Downstream Products

• 132119-61-0 1-(2-Benzyloxy-ethylsulfanylmethyl)-4,5-diphenyl-1H-[1,2,3]triazole 
• 132119-65-4 1-(2-Benzyloxy-ethylsulfanylmethyl)-1H-[1,2,3]triazole-4,5-dicarboxylic acid dimethyl ester 
• 132119-42-7 3-(2-Benzyloxy-ethylsulfanylmethyl)-3,6-dihydro-[1,2,3]triazolo[4,5-d]pyrimidin-7-one 
• 132119-54-1 1-(2-Benzyloxy-ethylsulfanylmethyl)-5-phenyl-1H-[1,2,3]triazole 
• 132119-55-2 1-(2-Benzyloxy-ethylsulfanylmethyl)-4-phenyl-1H-[1,2,3]triazole 
• 132119-41-6 1-(2-Benzyloxy-ethylsulfanylmethyl)-5-imino-2,5-dihydro-1H-[1,2,3]triazole-4-carboxylic acid amide 
• 132119-47-2 1-(2-Benzyloxy-ethylsulfanylmethyl)-1H-[1,2,3]triazole 
• 132119-39-2 <2-(benzyloxy)thioethoxy>triazomethane 

Relevant academic research and scientific papers

SYNTHESIS AND ANTIVIRAL ACTIVITY OF 1,2,3-TRIAZOLE AND 8-AZAPURINE DERIVATIVES BEARING ACYCLIC SUGARS

A variety of 1,2,3-triazole and 8-azapurine derivatives bearing acyclic sugar moieties were synthesized by the reaction of acyclic sugar azides with α-cyanoacetamide, norbornadiene, and acetylene derivatives, respectively.Antiviral tests of these compound

SELECTIVE DESULFURIZATION OF 1,3-DITHIANES, -OXATHIOLANES AND -THIAZOLIDINES BY TRIBUTYLTIN HYDRIDE

Selective desulfurization of 2-alkyl-1,3-dithianes, -oxathiolanes, or -thiazolidines 1 with one equivalent of tri-n-butyltin hydride yields acyclic compounds R1R2CHX(CH2)nSSnBu3 (X=S,O,NH; n=2,3), (2) which can be destannylated to the corresponding mercaptans 3.