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恶唑烷酮的合成:通过硅胶负载的高氯酸催化氨基酸衍生重氮酮的分子内环化反应

Synthesis of Oxazinanones: Intramolecular Cyclization of Amino Acid-Derived Diazoketones via Silica-Supported HClO Catalysis.

作者信息

Gallo Rafael D C, Campovilla Orlando C, Ahmad Anees, Burtoloso Antonio C B

机构信息

Instituto de Química de São Carlos, Universidade de São Paulo, São Carlos, Brazil.

出版信息

Front Chem. 2019 Feb 8;7:62. doi: 10.3389/fchem.2019.00062. eCollection 2019.

Abstract

A Brønsted acid catalyzed intramolecular cyclization of -Cbz-protected diazoketones, derived from α-amino acids, is described. The reaction proceeds under metal-free conditions and is promoted by ecofriendly silica-supported HClO as the catalyst and methanol as the solvent. This transformation enables the short synthesis of various 1,3-oxazinane-2,5-diones under mild reaction conditions and in good yields (up to 90%). The set-up is very simple; by just mixing all reagents together with no work-up necessary before purification, this protocol takes a greener approach.

摘要

描述了一种由α-氨基酸衍生的-Cbz保护的重氮酮的布朗斯特酸催化分子内环化反应。该反应在无金属条件下进行,以环境友好的硅胶负载高氯酸为催化剂、甲醇为溶剂促进反应。这种转化能够在温和的反应条件下以良好的产率(高达90%)短步骤合成各种1,3-恶嗪烷-2,5-二酮。实验装置非常简单;只需将所有试剂混合在一起,在纯化前无需后处理,该方法采用了更绿色的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4600/6376066/f5f5be78a113/fchem-07-00062-g0001.jpg

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