ID | 66645 |
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Author |
Abe, Takumi
Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
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Abstract | C3–N1′ bisindoles are unique structures, and the construction of these structures has drawn much attention. However, their synthesis still presents significant challenges that limit the functional group compatibility. This minireview summarizes the recent progress in the methodology for constructing C3–N1′ bisindoles. There are two approaches for access to C3–N1′ bisindoles: (1) direct approaches including reverse polarity techniques. (2) Stepwise approaches using designed and prefunctionalized substrates enable further functionalization by additional reactions to facilitate access to the target products. I believe that this review will allow its readers to develop novel approaches for the synthesis of C3–N1′ bisindoles.
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Note | This is an Accepted Manuscript of an article published by Royal Society of Chemistry (RSC).
This fulltext file will be available in Jan. 2025.
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Published Date | 2024
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Publication Title |
Organic and Biomolecular Chemistry
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Volume | volume22
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Issue | issue9
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Publisher | Royal Society of Chemistry (RSC)
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Start Page | 1756
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End Page | 1764
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ISSN | 1477-0520
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NCID | AA1168650X
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Content Type |
Journal Article
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language |
English
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OAI-PMH Set |
岡山大学
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Copyright Holders | © The Royal Society of Chemistry 2024
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File Version | author
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Related Url | isVersionOf https://doi.org/10.1039/d3ob02089d
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Funder Name |
Japan Society for the Promotion of Science
Takeda Science Foundation
Takahashi Industrial and Economic Research Foundation
Okayama Foundation for Science and Technology
Research Foundation for the Electrotechnology of Chubu
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助成番号 | 22K06503
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