α-氧基烯二硫缩醛的胶束溴化:通过酶催化温和和可扩展的方法。

IF 2.7 3区 化学 Q1 CHEMISTRY, ORGANIC
Thao Nguyen Thanh Huynh , Khuyen Thu Nguyen , Chisanu Krongyut , Rung-Yi Lai , Mongkol Sukwattanasinitt , Sumrit Wacharasindhu
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引用次数: 0

摘要

用KBr/H2O2催化了α-氧基烯酮二硫缩醛的溴化反应,并以不均匀曲霉的钒氯过氧化物酶(CiVCPO)为催化剂。一项使用2wt %表面活性剂TPGS-750-M的“在水中”和“在水中”酶促过程的比较研究表明,在水中方案不仅提供更高的产量,而且适应更广泛的底物范围。这种溴化方法在水胶束介质中制备了溴化α-氧基烯二硫缩醛,收率相当高(23个例子)。在胶束体系中,底物浓度增加到50 mM,溴化剂KBr和H2O2的量减少到约2.0当量,而效率不受影响。值得注意的是,该工艺允许以高收率制备克级溴化α-氧酮二硫缩醛。该方法的主要优点包括其良性和环保性,使用水作为绿色溶剂,并且具有大规模生产溴化α-氧基烯二硫缩醛的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Micelle-enabled bromination of α-oxo ketene dithioacetals: mild and scalable approach via enzymatic catalysis†

Micelle-enabled bromination of α-oxo ketene dithioacetals: mild and scalable approach via enzymatic catalysis†
The bromination of α-oxo ketene dithioacetals using KBr/H2O2, catalyzed by Curvularia inaequalis vanadium chloroperoxidase (CiVCPO), has been successfully demonstrated. A comparative study of enzymatic processes “on water” versus “in water”, using 2 wt% of the surfactant TPGS-750-M revealed that the in-water protocol not only provides higher yields but also accommodates a broader substrate scope. This bromination method in an aqueous micellar medium enabled the preparation of brominated α-oxo ketene dithioacetals in fair to excellent yields (23 examples). In the micellar system, the substrate concentration was increased up to 50 mM, and the amounts of the brominating agents KBr and H2O2 were reduced to approximately 2.0 equivalents without compromising efficiency. Notably, this process allows for the gram-scale preparation of brominated α-oxo ketene dithioacetals in high yields. Key advantages of this method include its benign and eco-friendly nature, the use of water as a green solvent, and its potential for large-scale production of brominated α-oxo ketene dithioacetals.
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来源期刊
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry 化学-有机化学
CiteScore
5.50
自引率
9.40%
发文量
1056
审稿时长
1.3 months
期刊介绍: Organic & Biomolecular Chemistry is an international journal using integrated research in chemistry-organic chemistry. Founded in 2003 by the Royal Society of Chemistry, the journal is published in Semimonthly issues and has been indexed by SCIE, a leading international database. The journal focuses on the key research and cutting-edge progress in the field of chemistry-organic chemistry, publishes and reports the research results in this field in a timely manner, and is committed to becoming a window and platform for rapid academic exchanges among peers in this field. The journal's impact factor in 2023 is 2.9, and its CiteScore is 5.5.
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