Benzoisoxazoles as Privileged Scaffolds in the Design and Synthesis of <i>N</i>‐containing Molecules: A Recent Update
Abstract Benzoisoxazoles, with a distinctive 10‐π‐electron system and significant polarity, readily trigger N −O bond cleavage, enabling multifaceted applications in organic synthesis. Over the past decade, the exponentially increased use of benzoisoxazoles towards the synthesis of highly valuable N ‐containing scaffolds, especially N ‐heterocycles, has garnered substantial attention. In this review, we summarize recent developments in the transformation of 2,1‐ and 1,2‐benzoisoxazoles since 2015, highlighting the neglected resemblances of these two nitroxy heterocycles. Key processes in the assorted reactions of benzoisoxazoles, including mechanisms, scope, catalyst‐controlled chemodivergence, current limitations, and developmental prospects, are also introduced and discussed.
Authors
- Nanjun Chen (ORCID: https://orcid.org/0000-0003-4074-5229)
- Xiaoqiang Guo (ORCID: https://orcid.org/0000-0002-1705-1977)
- Wenbo Ma (ORCID: https://orcid.org/0000-0002-9690-3639)
- Tai‐Ran Kang (ORCID: https://orcid.org/0000-0001-6851-2967)
- Peng Sun (ORCID: https://orcid.org/0000-0003-0348-5405)
Institutions
- Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
- Chengdu University (CN)
Publication Details
- Journal
- European Journal of Organic Chemistry
- Published
- 2024-12-04
- DOI
- https://doi.org/10.1002/ejoc.202401021
- Citations
- 4
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 1.00