1498288-77-9

Upstream product

• 51-35-4 4R-4-hydroxyproline 
• 1360588-94-8 (6R,7aS)-1,1-bis[3,5-bis(trifluoromethyl)phenyl]-6-hydroxytetrahydropyrrolo[1,2-c]oxazol-3(1H)-one 
• 1498288-74-6 (6S,7aS)-6-azido-1,1-bis[3,5-bis(trifluoromethyl)phenyl]tetrahydropyrrolo[1,2-c]oxazol-3(1H)-one 
• 1498288-75-7 (6S,7aS)-6-amino-1,1-bis[3,5-bis(trifluoromethyl)phenyl]tetrahydropyrrolo[1,2-c]oxazol-3(1H)-one 
• 1498288-73-5 (6R,7aS)-1,1-bis[3,5-bis(trifluoromethyl)phenyl]-3-oxohexahydropyrrolo[1,2-c]oxazol-6-yl methanesulfonate 
• 83487-17-6 (2S,4R)-(-)-N-methyloxycarbonyl-4-hydroxypyrrolidine-2-carboxylic acid methyl ester 

Downstream Products

• 1498288-86-0 C₃₀H₃₄F₁₂N₂O 
• 1498288-87-1 C₃₂H₄₀F₁₂N₂OSi 
• 1498288-81-5 C₂₉H₃₂F₁₂N₂O 
• 1498288-89-3 C₃₅H₄₆F₁₂N₂OSi 
• 1498288-88-2 C₃₅H₄₆F₁₂N₂OSi 

Relevant academic research and scientific papers

Optimizing the structure of 4-dialkylamino-α,α-diarylprolinol ethers as catalysts for the enantioselective cyclopropanation of α,β-unsaturated aldehydes in water

We optimized the structure of a new family of chiral diarylprolinol-type organocatalysts with improved performances in conjugate addition reactions performed in water and proceeding under the iminium activation manifold. The principles behind the catalyst