370857-89-9

Upstream product

• 628-21-7 1,4-Diiodobutane 
• 370857-87-7 N-((R)-2-Mercapto-1-{(S)-1-[(R)-1-(methoxy-methyl-carbamoyl)-2-tritylsulfanyl-ethylcarbamoyl]-ethylcarbamoyl}-ethyl)-benzamide 
• 370857-88-8 N-((R)-2-(4-Bromo-butylsulfanyl)-1-{(S)-1-[(R)-1-(methoxy-methyl-carbamoyl)-2-tritylsulfanyl-ethylcarbamoyl]-ethylcarbamoyl}-ethyl)-benzamide 
• 370857-84-4 {(S)-1-[(R)-1-(Methoxy-methyl-carbamoyl)-2-tritylsulfanyl-ethylcarbamoyl]-ethyl}-carbamic acid 9H-fluoren-9-ylmethyl ester 
• 370857-83-3 Fmoc-Cys(Trt)-N(CH₃)-OCH₃ 

Relevant academic research and scientific papers

General method for the synthesis of cyclic peptidomimetic compounds

A number of cyclic peptides, wherein the i and i+1 residue side chains are joined by an alkyl linker and a Weinreb amide is present at the C-terminus, were synthesized. Using LiCl to solubilize these peptides in THF the C-terminus can be readily converted to an activated carbonyl such as an aldehyde or ketone.