Sabir Shekh, Pandey Chandra Bhan, Yadav Ajay K, Tiwari Bhoopendra, Jat Jawahar L
Department of Chemistry , Baba Saheb Bhim Rao Ambedkar University , Lucknow 226025 , India.
Division of Molecular Synthesis & Drug Discovery , Centre of Biomedical Research , SGPGIMS-Campus, Raebareli Road , Lucknow 226014 , India.
J Org Chem. 2018 Oct 5;83(19):12255-12260. doi: 10.1021/acs.joc.8b01673. Epub 2018 Sep 17.
Unactivated aziridines are the core substructures in a plethora of bioactive natural products and serve as building blocks in organic synthesis. Despite this, very limited methods are available to access them directly from olefins, as most of the known methods are devoted to their activated counterparts. Herein, we have developed a highly efficient Rh(II)-catalyzed method for the direct preparation of unactivated aziridines from olefins using O-(sulfonyl)hydroxylamines as the aminating agent. The reactions proceed with a high stereospecificity.
未活化的氮杂环丙烷是众多生物活性天然产物中的核心子结构,并且在有机合成中用作构建单元。尽管如此,直接从烯烃制备未活化氮杂环丙烷的方法非常有限,因为大多数已知方法都致力于制备其活化形式的氮杂环丙烷。在此,我们开发了一种高效的铑(II)催化方法,以O-(磺酰基)羟胺作为胺化剂,直接从烯烃制备未活化的氮杂环丙烷。反应具有高立体专一性。