Peroxygenase‐Enabled Reductive Kinetic Resolution for the Enantioenrichment of Organoperoxides

Author:

Shen Qianqian12,Yan Juzhang1,Han Yuchen1,Zhang Zaoxiao2,Li Huanhuan1,Kong Dulin3,Shi Jianjun4,Cui Chengsen1,Zhang Wuyuan1ORCID

Affiliation:

1. Key Laboratory of Engineering Biology for Low-carbon Manufacturing Tianjin Institute of Industrial Biotechnology Chinese Academy of Sciences 32 West 7th Avenue Tianjin 300308 China

2. School of Chemical Engineering and Technology Xi'an Jiaotong University Xi'an 710049 China

3. School of Pharmacy Hainan Medical University Haikou 571199, Hainan China

4. College of Chemistry and Chemical Engineering Hainan Normal University Haikou 571158, Hainan China

Abstract

AbstractEnantiomerically pure organoperoxides serve as valuable precursors in organic transformations. Herein, we present the first examples of unspecific peroxygenase catalyzed kinetic resolution of racemic organoperoxides through asymmetric reduction. Through meticulous investigation of the reaction conditions, it is shown that the unspecific peroxygenase from Agrocybe aegerita (AaeUPO) exhibits robust catalytic activity in the kinetic resolution reactions of the model substrate with turnover numbers up to 60000 and turnover frequency of 5.6 s−1. Various aralkyl organoperoxides were successfully resolved by AaeUPO, achieving excellent enantioselectivities (e.g., up to 99 % ee for the (S)‐organoperoxide products). Additionally, we screened commercial peroxygenase variants to obtain the organoperoxides with complementary chirality, with one mutant yielding the (R)‐products. While unspecific peroxygenases have been extensively demonstrated as a powerful oxidative catalysts, this study highlights their usefulness in catalyzing the reduction of organoperoxides and providing versatile chiral synthons.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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