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利用氧化亚胺极性翻转的N-杂环卡宾催化用于生成亚胺基唑鎓盐。

N-Heterocyclic Carbene Catalysis Exploiting Oxidative Imine Umpolung for the Generation of Imidoyl Azoliums.

作者信息

Das Tamal Kanti, Madica Krishnaprasad, Krishnan Jagadeesh, Marelli Udaya Kiran, Biju Akkattu T

机构信息

Organic Chemistry Division, CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, Pune 411008, India.

Academy of Scientific and Innovative Research (AcSIR), New Delhi 110020, India.

出版信息

J Org Chem. 2020 Apr 3;85(7):5114-5121. doi: 10.1021/acs.joc.0c00360. Epub 2020 Mar 20.

Abstract

Although NHC-catalyzed umpolung of imines are known, the related reactions under oxidative conditions are limited. Described herein is the two-step process involving the initial formation of aldimines from the corresponding aldehydes and 2-amino benzyl alcohols followed by NHC-catalyzed cyclization proceeding via the imidoyl azoliums under oxidative conditions. The reaction allowed the synthesis of trifluoromethylated 3,1-benzoxazines in good yields and broad scope. The role of NHC in the intramolecular cyclization and preliminary mechanistic experiments are also provided.

摘要

尽管已知氮杂环卡宾催化的亚胺极性反转反应,但氧化条件下的相关反应却很有限。本文描述了一个两步过程,首先由相应的醛和2-氨基苄醇生成醛亚胺,然后在氧化条件下通过亚胺酰基唑鎓盐进行氮杂环卡宾催化的环化反应。该反应能够以良好的产率和广泛的底物范围合成三氟甲基化的3,1-苯并恶嗪。还提供了氮杂环卡宾在分子内环化反应中的作用以及初步的机理实验。

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