1321925-52-3

Upstream product

• 1321925-40-9 methyl (1S,2R)-2-(tert-butoxycarbonylamino)cyclohex-4-enecarboxylate 
• 1321925-41-0 methyl (1S,2R,4S,5R)-2-(tert-butoxycarbonylamino)-4,5-epoxycyclohexanecarboxylate 
• 1321925-49-8 methyl (1S,2R,4R,5R)-2-(tert-butoxycarbonylamino)-4-(2-chloroethoxy)-5-hydroxycyclohexanecarboxylate 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 31139-02-3 (1R,6S)-6-methoxycarbonyl-3-cyclohexene-1-carboxylic acid 
• 503167-42-8 (1S,6R)-6-Isocyanato-cyclohex-3-enecarboxylic acid methyl ester 
• 935-79-5 cis-1,2,3,6-tetrahydrophthalic anhydride 

Downstream Products

• 1321925-38-5 methyl (1S,2R,4R,5R)-4-(2-azidoethoxy)-2-(tert-butoxycarbonylamino)-5-(tert-butyldimethylsilanyloxy)cyclohexanecarboxylate 

Relevant academic research and scientific papers

2-Azidoethoxy derivatives of 2-aminocyclohexanecarboxylic acids (ACHC): Interesting building blocks for the synthesis of cyclic β-peptide conjugates

Oligomers of cyclic-β-aminoacids possess a high resistance to peptidase-catalyzed hydrolysis and display a high intrinsic tendency to adopt regular secondary structures. These characteristics are attractive to develop new biologically active substances. H