372965-96-3

Upstream product

• 372965-98-5 Benzhydrylidene-{4-[(S)-((2R,4S,5R)-5-ethyl-1-aza-bicyclo[2.2.2]oct-2-yl)-triisopropylsilanyloxy-methyl]-quinolin-6-yl}-amine 
• 372965-97-4 Trifluoro-methanesulfonic acid 4-[(S)-((2R,4S,5R)-5-ethyl-1-aza-bicyclo[2.2.2]oct-2-yl)-triisopropylsilanyloxy-methyl]-quinolin-6-yl ester 
• 372966-04-6 dihydrocupreidine monotriflate 
• 1013-88-3 Benzophenone imine 

Relevant academic research and scientific papers

Highly effective transition structure designed catalyst for the enantio- and position-selective dihydroxylation of polyisoprenoids.

[structure: see text] The chiral monocinchona derivative shown, synthesized in one step from two efficiently prepared chiral building blocks, was designed under mechanistic guidance as a catalyst for the enantio- and position-selective dihydroxylation of the terminal isopropylidene group of polyisoprenoids. Its efficacy as a synthetic reagent for this purpose was demonstrated for several different substrates.