503182-60-3

Upstream product

• 503182-59-0 Z-T(tBu)E(tBu)VD(tBu)-OMe 
• 103213-32-7 N-(9-fluorenylmethoxycarbonyl)-S-trityl-L-cysteine 
• 503182-48-7 methyl ((benzyloxy)carbonyl)-L-valyl-L-(O-tert-butyl)threoninate 
• 3886-08-6 5-tert-butyl N-benzyloxycarbonyl-L-glutamate 
• 39895-10-8 L-aspartic acid β-tert-butyl ester α-methyl ester 
• 1149-26-4 (S)-N-(benzyloxycarbonyl)valine 
• 204919-57-3 methyl ((benzyloxy)carbonyl)-L-valyl-L-(O-tert-butyl)aspartate 
• 206865-05-6 Z-E(tBu)VD(tBu)-OMe 

Relevant academic research and scientific papers

A facile synthetic method to prepare fluorescently labeled ROMP polymers

(Chemical Equation Presented) To probe the activities of sperm ADAM protein (fertilinβ), we devised a general synthetic strategy to generate fluorescently labeled fertilinβ oligopeptide polymers. Immunofluorescence studies with these polymers demonstrated that fertilinβ polymers bind specifically to a protein receptor on the mouse egg plasma membrane.

Increased polymer length of oligopeptide-substituted polynorbornenes with LiCl

The ring-opening metathesis polymerization (ROMP) reaction is extraordinarily useful for the preparation of a large variety of polymers. We report that the length (n = 25-50) of high-substituent-density oligopeptide polymers synthesized by ROMP is dramati