871915-41-2

Upstream product

• 871915-37-6 H2N-Phe-Phe-Gly-Thr(Ψ^Me,MePro)-Phe-Phe-Gly-OH 
• 871915-43-4 Cbz-Gly-Thr(Ψ^Me,MePro)-OMe 
• 871915-38-7 Cbz-Gly-Thr(Ψ^Me,MePro)-OH 
• 51165-32-3 Cbz-Phe-Phe-Gly-OMe 
• 871915-39-8 Cbz-Gly-Thr(Ψ^Me,MePro)-Phe-Phe-Gly-OMe 
• 871915-46-7 H2N-Phe-Gly-Thr(Ψ^Me,MePro)-Phe-Phe-Gly-OMe 
• 871915-45-6 Cbz-Phe-Gly-Thr(Ψ^Me,MePro)-Phe-Phe-Gly-OMe 
• 871915-40-1 Cbz-Phe-Phe-Gly-Thr(Ψ^Me,MePro)-Phe-Phe-Gly-OMe 
• 871915-47-8 Cbz-Phe-Phe-Gly-Thr(Ψ^Me,MePro)-Phe-Phe-Gly-OH 
• 41961-03-9 Cbz-Gly-L-Thr-OMe 
• 1161-13-3 N-Cbz-L-Phe 
• 5184-17-8 N-benzyloxycarbonyl-L-phenylalanylglycine methyl ester 
• 105224-80-4 H₂N-Phe-Phe-Gly-OMe 
• 65559-51-5 L-Phenylalaninyl-glycine methyl ester 

Relevant academic research and scientific papers

N,O-isopropylidenated threonines as tools for peptide cyclization: Application to the synthesis of mahafacyclin B

(Chemical Equation Presented) The influence of a single N,O-isopropylidenated threonine turn-inducer on the cyclization of a linear heptapeptide precursor to mahafacyclin B has been investigated. Incorporation of an N,O-isopropylidenated threonine more th