871915-38-7

Upstream product

• 41961-03-9 Cbz-Gly-L-Thr-OMe 
• 871915-43-4 Cbz-Gly-Thr(Ψ^Me,MePro)-OMe 

Downstream Products

• 871915-47-8 Cbz-Phe-Phe-Gly-Thr(Ψ^Me,MePro)-Phe-Phe-Gly-OH 
• 871915-40-1 Cbz-Phe-Phe-Gly-Thr(Ψ^Me,MePro)-Phe-Phe-Gly-OMe 
• 871915-37-6 H2N-Phe-Phe-Gly-Thr(Ψ^Me,MePro)-Phe-Phe-Gly-OH 
• 871915-42-3 H₂N-Phe-Phe-Gly-Thr-Phe-Phe-Gly-OH 
• 871915-41-2 cyclo-[Phe-Phe-Gly-Thr(Ψ^Me,MePro)-Phe-Phe-Gly] 
• 871915-45-6 Cbz-Phe-Gly-Thr(Ψ^Me,MePro)-Phe-Phe-Gly-OMe 
• 871915-46-7 H2N-Phe-Gly-Thr(Ψ^Me,MePro)-Phe-Phe-Gly-OMe 
• 871915-44-5 H2N-Gly-Thr(Ψ^Me,MePro)-Phe-Phe-Gly-OMe 
• 871915-39-8 Cbz-Gly-Thr(Ψ^Me,MePro)-Phe-Phe-Gly-OMe 

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

Total Synthesis of the Proposed Microcyclamides MZ602 and MZ568

The first convergent total synthesis for the proposed structures of microcyclamides MZ602 (1) and MZ568 (2) has been accomplished in 11 linear steps with 12.5 and 16.8% overall yield, respectively. Key features of the syntheses include a one-pot cascade r