Taming glycosylidene carbenes through bench-stable glycosylidene diaziridines to access boro-ketosides

IF 11.5 Q1 CHEMISTRY, PHYSICAL
Charles C.J. Loh
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引用次数: 0

Abstract

In this issue of Chem Catalysis, He and co-workers demonstrate easy access to diverse glycosyl boro-ketosides via a rare glycosylidene carbene intermediate. They use stable glycosylidene diaziridines as precursors for carbene generation, leading to products convertible into rare sugars and pharmaceutically interesting derivatives, such as tofogliflozin.

通过稳定的糖基二氮杂环丁烷驯服糖基碳烯,从而获得硼酮苷
在本期的《化学催化》(Chem Catalysis)杂志上,He 和合作者展示了通过一种罕见的亚基碳烯中间体轻松获得多种糖基硼酮苷(glycosyl boro-ketosides )的方法。他们使用稳定的亚基二氮杂环胺作为生成碳烯的前体,从而得到了可转化为稀有糖类和药物学上有趣的衍生物的产物,例如托非格列净。
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来源期刊
CiteScore
10.50
自引率
6.40%
发文量
0
期刊介绍: Chem Catalysis is a monthly journal that publishes innovative research on fundamental and applied catalysis, providing a platform for researchers across chemistry, chemical engineering, and related fields. It serves as a premier resource for scientists and engineers in academia and industry, covering heterogeneous, homogeneous, and biocatalysis. Emphasizing transformative methods and technologies, the journal aims to advance understanding, introduce novel catalysts, and connect fundamental insights to real-world applications for societal benefit.
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