Related Products of 224434-01-9《Chiral Alkyl Amine Synthesis via Catalytic Enantioselective Hydroalkylation of Enecarbamates》 was published in 2021. The authors were Qian, Deyun;Bera, Srikrishna;Hu, Xile, and the article was included in《Journal of the American Chemical Society》. The author mentioned the following in the article:
A nickel-catalyzed hydroalkylation method to assemble a wide range of chiral alkyl amines from enecarbamates (N-Cbz-protected enamines) and alkyl halides with high regio- and enantioselectivity was reported. The method works for both nonactivated and activated alkyl halides and was able to produce enantiomerically enriched amines with two minimally differentiated α-alkyl substituents. The mild conditions led to high functional group tolerance, which is demonstrated in the postproduct functionalization of many natural products and drug mols., as well as the synthesis of chiral building blocks and key intermediates to bioactive compounds And (S)-2-Amino-2-(4-fluorophenyl)ethanol (cas: 224434-01-9) was used in the research process.
(S) – 2-amino-2 – (4-fluorophenyl) ethanol (cas: 224434-01-9) has the characteristics of alcohol. In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. Related Products of 224434-01-9
Reference:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts