E-viri
Recenzirano
-
Horino, Satoshi; Nishio, Tomoya; Kawanishi, Shinji; Oki, Shinya; Nishihara, Koichi; Ikawa, Takashi; Kanomata, Kyohei; Wagner, Karla; Gröger, Harald; Akai, Shuji
Chemistry : a European journal, October 26, 2022, 2022-10-26, Letnik: 28, Številka: 60Journal Article
A method for enantiodivergent production of S and R propargylic alcohols from their racemates by using commercial lipase‐based dynamic kinetic resolution achieves quantitative conversion of the racemates into optically pure substances. The right and left hands, wearing jeweled rings indicating individual reaction steps, lead to opposite enantioselection, producing S and R alcohols, respectively. The order of the jewels is key to the enantioswitch. More information can be found in the Research Article by S. Akai and co‐workers (DOI: 10.1002/chem.202202437).
