1498288-91-7

Upstream product

• 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 
• 1498288-74-6 (6S,7aS)-6-azido-1,1-bis[3,5-bis(trifluoromethyl)phenyl]tetrahydropyrrolo[1,2-c]oxazol-3(1H)-one 
• 1498288-78-0 C₃₄H₃₈F₁₂N₂O₂ 
• 1498288-82-6 C₃₃H₄₀F₁₂N₂O 
• 79271-56-0 triethylsilyl trifluoromethyl sulfonate 
• 1360588-94-8 (6R,7aS)-1,1-bis[3,5-bis(trifluoromethyl)phenyl]-6-hydroxytetrahydropyrrolo[1,2-c]oxazol-3(1H)-one 
• 51-35-4 4R-4-hydroxyproline 

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