134360-52-4

Upstream product

• 57260-73-8 N-BOC-1,2-diaminoethane 
• 98-59-9 p-toluenesulfonyl chloride 
• 24424-99-5 di-tert-butyl dicarbonate 
• 14316-16-6 N-tosylethylenediamine 

Downstream Products

• 1020203-69-3 C₂₁H₂₉N₃O₅S 
• 1020203-68-2 C₃₁H₃₅N₃O₅S 
• 1020203-70-6 C₂₁H₂₉N₃O₆S 
• 1020203-66-0 (E)-N,N-diethyl-[3-(tert-butyloxycarbonyl)-1-(p-toluenesulfonyl)imidazolidin-2-ylidene]acetamide 
• 1160241-95-1 tert-butyl 2-(4-methyl-N-(prop-2-ynyl)-phenylsulfonamido)ethylcarbamate 
• 1429060-05-8 tert-butyl 2-(N-ethynyl-4-methylphenylsulfonamido)ethylcarbamate 
• 1429060-08-1 tert-butyl 4-tosyl-3,4-dihydropyrazine-1(2H)-carboxylate 
• 1429060-06-9 tert-butyl 2-(4-methyl-N-(phenylethynyl)phenylsulfonamido)ethylcarbamate 
• 1429060-19-4 tert-butyl 6-phenyl-4-tosyl-3,4-dihydropyrazine-1(2H)-carboxylate 

Relevant academic research and scientific papers

Development of an endoplasmic reticulum-targeting fluorescent probe for the imaging of polarity in living cells and tissues

Cell polarity is one of the important parameters of the biological microenvironment and controls the synthesis of functional proteins. As one of the key links in protein synthesis, the endoplasmic reticulum is highly sensitive to the cellular environment

Chemoselective alkynylation of N-sulfonylamides versus amides and carbamates-Synthesis of tetrahydropyrazines

The chemoselective alkynylation of N-sulfonylamides versus amides and carbamates using TMS-EBX as an alkynylating agent leads to the formation of non-symmetrical tetrahydropyrazines from orthogonally protected diamines. The Royal Society of Chemistry 2013

Gold(1)-catalyzed intramolecular dihydroamination of allenes with N,N′-disubstituted ureas to form bicyclic imidazolidin-2-ones

Reaction of W-δ-allenyl urea 1 with a catalytic 1:1 mixture of gold(1) N-heterocyclic carbene complex (5)AuCI [5 = 1,3-bis(2,6- diisopropylphenyl)imidazol-2-ylidine] and AgPF6 at room temperature for 2 h led to isolation of bicyclic imidazolidi