Synthetic Route of 176706-98-2, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.176706-98-2, Name is 2,2-Bis[(4S)-4-benzyl-2-oxazolin-2-yl]propane, molecular formula is C23H26N2O2. In a Patent，once mentioned of 176706-98-2
The invention discloses a asymmetric catalytic synthesis of (R)- 4, 7 – dimethyl – 1 – Tetralone method. This method utilizes the dual oxazoline/cobalt catalytic racemic 2 – halogenating third ester and methyl phenyl Grignard reagent asymmetric Kumada cross-coupling reaction, to Mr. (S)- toluene c ester 2. Then diisobutyl hydride (DIBAL – H) aluminum is reduced to (S) tolyl propyl alcohol – to 3, then bromo, and vinyl Grignard reagent coupled to obtain the (R)- 4 – methylphenyl – 1 – pentene 5. Subsequently carries out the oxidation reaction with borohydride – Dess – Martin oxidation reaction, to obtain the (R)- 4 – methylphenyl pentanals 6. The final silver oxide oxidation, by Fourier acylation reaction in the molecule, the ring synthesis of (R)- 4, 7 – dimethyl – 1 – Tetralone. Synthetic route of this invention is simple, a total of 8 step reaction, the total yield is 27%, optical purity of the product is 90%. (by machine translation)
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Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI