89902-54-5

Upstream product

• 67-56-1 methanol 
• 455-19-6 4-Trifluoromethylbenzaldehyde 
• 25616-13-1 alanine hydrochloride 
• 13515-97-4 methyl 2-aminopropanoate monohydrochloride 

Downstream Products

• 89902-60-3 methyl c-4-(4-trifluoromethylphenyl)-2-methyl-7-phenyl-6,8-dioxo-3,7-diazabicyclo<3.3.0>octane-r-2-carboxylate 
• 1431318-86-3 (1'S,2S,3'R,3a'S,7a'R)-methyl 3'-methyl-5,7'-dioxo-1'-(4-(trifluoromethyl)phenyl)-1',2',3',3a',4,5,7',7a'-octahydro-3H-spiro[furan-2,4'-isoindole]-3'-carboxylate 
• 1370441-33-0 C₃₀H₂₈F₆N₂O₆ 

Relevant academic research and scientific papers

Biology-oriented synthesis of benzopyrano[3,4-c]pyrrolidines

A natural product inspired synthesis of 6,6,5-tricyclic compounds via a silver(I)-catalyzed formal 1,3-dipolar cycloaddition of coumarins with α-iminoesters was developed. The reaction proceeds in a stepwise reaction course under formation of the trans-su

X=Y-ZH Systems as Potential 1,3-Dipoles. Part 1. Background and Scope

X=Y-ZH Systems are considered in general terms and divided into four classes according to the number of constituent atoms that possess lone-pair electrons.Those systems in which the central Y atom possesses a lone pair are shown to be capable of participa