1356115-96-2

Upstream product

• 501096-26-0 (2RS,5S)-1-(tert-butoxycarbonyl)-2-phenyl-5-carbomethoxy-3-pyrroline 
• 1356154-61-4 C₁₇H₂₃NO₆ 
• 1356116-16-9 5-tert-butyl 4-methyl (3aR,4S,6S,6aS)-2,2-dimethyl-6-phenyldihydro-3aH-[1,3]dioxolo[4,5-c]pyrrole-4,5(4H)-dicarboxylate 
• 1356115-99-5 C₁₉H₂₅NO₅ 
• 188945-41-7 ethyl di-O-tolylphosphonoacetate 

Downstream Products

• 1356115-98-4 (Z)-3-[(2R,3R,4S,5S)-1-(tert-butoxycarbonyl)-3,4-dihydroxy-5-phenylpyrrolidin-2-yl]acrylic acid 
• 1356116-02-3 ethyl 3-[(2R,3R,4S,5S)-3,4-dihydroxy-5-phenylpyrrolidin-2-yl]propanoate 
• 1356116-04-5 tert-butyl (3aR,4R,6S,6aS)-4-(3-ethoxy-3-oxopropyl)-2,2-dimethyl-6-phenyldihydro-3aH-[1,3]dioxolo[4,5-c]pyrrole-5(4H)-carboxylate 
• 1356116-20-5 tert-butyl (2R,3R,4S,5S)-2-[(Z)-3-ethoxy-3-oxoprop-1-enyl]-3,4-dihydroxy-5-phenylpyrrolidine-1-carboxylate 

Relevant academic research and scientific papers

Stereoselective synthesis of aza analogues of isoaltholactone and goniothalesdiol - New applications of the Heck-Matsuda reaction

The stereoselective synthesis of nitrogen analogues of biologically active isoaltholactone and goniothalesdiol are described. The successful strategy employed a Heck-Matsuda reaction between a chiral endocyclic enecarbamate bearing an ester functionality