1444003-19-3

Upstream product

• 63-91-2 L-phenylalanine 
• 551-93-9 2-aminoacetophenone 
• 46687-57-4 (S)-3-phenyl-2-(1H-pyrrol-1-yl)propanoic acid 

Downstream Products

• 1444003-09-1 C₂₄H₂₉N₃O₃ 
• 1444003-10-4 3S,5R,7R,8R,11R-5,8-dihydroxy-5-(4-oxo-3H-quinqzolin-3-yl)-3-benzyl-8-methyl-9,10-benzo-2-oxo-1,4-diazatricyclo[5.3.1.0^4,11]undec-9-ene 
• 1444003-05-7 C₂₇H₂₆N₂O₆ 
• 1444003-06-8 dimethyl (3S,9S,10R,17R)-3-benzyl-10-hydroxy-10-methyl-2-oxo-1,4-diazatetracyclo[7.7.1.0^4,17]heptadeca-5,7,11,13,15-pentaene-6,7-dicarboxylate 

Relevant academic research and scientific papers

Photoassisted synthesis of enantiopure alkaloid mimics possessing unprecedented polyheterocyclic cores

Enantiopure alkaloid mimics are synthesized via high yielding intramolecular cycloadditions of photogenerated azaxylylenes tethered to pyrroles, with further growth of molecular complexity via post-photochemical transformations of primary photoproducts. This expeditious access to structurally unprecedented polyheterocyclic cores is being developed in the context of diversity-oriented synthesis, as the modular design allows for rapid "pre-assembly" of diverse photoprecursors from simple building blocks/diversity inputs.