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ID 66645
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Author
Abe, Takumi Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University ORCID Kaken ID researchmap
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.
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.
Published Date
2024
Publication Title
Organic and Biomolecular Chemistry
Volume
volume22
Issue
issue9
Publisher
Royal Society of Chemistry (RSC)
Start Page
1756
End Page
1764
ISSN
1477-0520
NCID
AA1168650X
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© The Royal Society of Chemistry 2024
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DOI
Web of Science KeyUT
Related Url
isVersionOf https://doi.org/10.1039/d3ob02089d
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
助成番号
22K06503