化学
酮
转鼓
产量(工程)
苯甲醛
安息香
有机化学
催化作用
冶金
亲核细胞
材料科学
作者
Zhiran Ju,Zhiyun Li,Menglan Li,Saili Xu,Kumaravel Kaliaperumal,Fen‐Er Chen
标识
DOI:10.1021/acs.joc.3c01641
摘要
Herein, we present a novel and ecofriendly biocatalytic approach for synthesizing efinaconazole (7), a clinically used antifungal agent. This method involves utilizing benzaldehyde lyase (BAL) to catalyze the crucial benzoin condensation step in the ketone precursor. Treating 2,4-difluorobenzaldehyde with BAL in the presence of thiamin-diphosphate (ThDP) and Mg2+ resulted in the formation of α-hydroxy ketone which then underwent the preparation of 7. This innovative approach not only provides a greener alternative but also offers significant advantages over the traditional chemical process. Through our efforts and development work, we have established efficient and scalable procedures that enable the production of 7 in a moderate 38% yield.
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