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(R)-(-)-2-TERT-BUTYLAMINO-1-PHENYLETHAN& synthesis

5synthesis methods
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Yield:14467-51-7 95 %

Reaction Conditions:

with bis(1,5-cyclooctadiene)diiridium(I) dichloride;hydrogen;C36H41FeN2O2PS;sodium hydroxide in 1,2-dichloro-ethane;isopropyl alcohol at 25 - 30; under 30003 Torr;Schlenk technique;Autoclave;

References:

Zhang, Lei;Cao, Liming;Sun, Maolin;Liang, Chaoming;Yang, Lei;Ma, Yueyue;Cheng, Ruihua;Ye, Jinxing [Chemistry - A European Journal,2023] Location in patent:supporting information