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使用高价碘介导的 NH 转移合成亚砜亚胺和磺酰胺。

Synthesis of Sulfoximines and Sulfonimidamides Using Hypervalent Iodine Mediated NH Transfer.

机构信息

Department of Pharmacy-Drug Sciences University of Bari "A. Moro" Via E. Orabona 4, 70125 Bari, Italy.

Department of Chemistry, Imperial College London, Molecular Sciences Research Hub, London W12 0BZ, UK.

出版信息

Molecules. 2023 Jan 22;28(3):1120. doi: 10.3390/molecules28031120.

Abstract

The development of NH transfer reactions using hypervalent iodine and simple sources of ammonia has facilitated the synthesis of sulfoximines and sulfonimidamides for applications across the chemical sciences. Perhaps most notably, the methods have been widely applied in medicinal chemistry and in the preparation of biologically active compounds, including in the large-scale preparation of an API intermediate. This review provides an overview of the development of these synthetic methods involving an intermediate iodonitrene since our initial report in 2016 on the conversion of sulfoxides into sulfoximines. This review covers the NH transfer to sulfoxides and sulfinamides, and the simultaneous NH/O transfer to sulfides and sulfenamides to form sulfoximines and sulfonimidamides, respectively. The mechanism of the reactions and the identification of key intermediates are discussed. Developments in the choice of reagents, and in the reaction conditions and setups used are described.

摘要

使用高价碘和简单氨源发展 NH 转移反应促进了亚砜亚胺和磺酰胺的合成,在化学科学的各个领域都有应用。值得注意的是,这些方法已被广泛应用于药物化学和生物活性化合物的制备,包括 API 中间体的大规模制备。自 2016 年我们首次报道亚砜转化为亚砜亚胺以来,本综述概述了涉及碘硝𬭩中间体的这些合成方法的发展。本综述涵盖了 NH 向亚砜和亚磺酰胺的转移,以及向硫化物和亚磺酰胺的同时 NH/O 转移,分别形成亚砜亚胺和磺酰胺。讨论了反应机理和关键中间体的鉴定。描述了试剂选择以及反应条件和设置的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d31/9920176/d2ad81c82638/molecules-28-01120-g001.jpg

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