生物催化
化学
半乳糖氧化酶
产量(工程)
氧化还原
组合化学
有机化学
过程开发
酶
催化作用
材料科学
反应机理
工艺工程
工程类
冶金
作者
Megan H. Shaw,Anna Fryszkowska,Oscar Alvizo,Ilana Attadgie,Margie Borra‐Garske,Paul N. Devine,Da Duan,Shane T. Grosser,Jacob H. Forstater,G. Hughes,Kevin M. Maloney,Eric L. Margelefsky,Keith Mattern,Margaret T. Miller,Christopher C. Nawrat,Jovana Nazor,Peter Orth,Claire M. Ouimet,Sandra A. Robaire,Serge Ruccolo
标识
DOI:10.1021/acs.oprd.4c00075
摘要
Biocatalytic oxidations have the potential to address many synthetic challenges, enabling the selective synthesis of chiral intermediates, such as carbonyl compounds, alcohols, or amines. The use of oxygen-dependent enzymes can dramatically reduce the environmental footprint of redox transformations at the manufacturing scale. Here, as part of the biocatalytic cascade to the anti-HIV investigational drug islatravir (1), we describe the development of an aerobic oxidation process delivering (R)-ethynylglyceraldehyde-3-phosphate (3) using an evolved galactose oxidase enzyme. Integrated enzyme and reaction engineering were critical for achieving a robust, high-yielding oxidation performed at pilot-plant scale (>20 kg, 90% yield).
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