1532518-99-2

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 1532518-98-1 di-tert-butyl (2R,3S,4S)-3-(2-(tert-butoxy)-2-oxoethyl)-4-(2-methoxyphenyl)pyrrolidine-1,2-dicarboxylate 
• 328-50-7 α-ketoglutaric acid 
• 1532518-96-9 di-tert-butyl (S)-3-((S)-1-(2-methoxyphenyl)-2-nitroethyl)-2-oxopentanedioate 

Downstream Products

• 132785-33-2 MFPA 
• 1532519-00-8 di-tert-butyl (2S,3S,4S)-3-(2-(tert-butoxy)-2-oxoethyl)-4-(5-iodo-2-methoxyphenyl)pyrrolidine-1,2-dicarboxylate 
• 1532519-01-9 di-tert-butyl (2S,3S,4S)-3-(2-(tert-butoxy)-2-oxoethyl)-4-(5-(3-hydroxyprop-1-yn-1-yl)-2-methoxyphenyl)pyrrolidine-1,2-dicarboxylate 
• 1532519-05-3 di-tert-butyl (2S,3S,4S)-4-(5-(3-azidoprop-1-yn-1-yl)-2-methoxyphenyl)-3-(2-(tert-butoxy)-2-oxoethyl)pyrrolidine-1,2-dicarboxylate 
• 1532519-02-0 di-tert-butyl (2S,3S,4S)-4-(5-(3-aminopropyl)-2-methoxyphenyl)-3-(2-(tert-butoxy)-2-oxoethyl)pyrrolidine-1,2-dicarboxylate 
• 1532519-04-2 C₃₈H₃₆N₂O₉ 

Relevant academic research and scientific papers

Practical synthesis of Kainoids: A new chemical probe precursor and a fluorescent probe

A practical total synthesis of kainoid MFPA (5) was achieved in only six steps, via a novel Ni-catalyst-mediated asymmetric conjugate addition reaction. Furthermore, a fluorescein-based fluorescent ionotropic glutamate receptor probe 28 was efficiently sy