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ID 66645
フルテキストURL
著者
Abe, Takumi Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University ORCID Kaken ID researchmap
抄録
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.
備考
This is an Accepted Manuscript of an article published by Royal Society of Chemistry (RSC).
This fulltext file will be available in Jan. 2025.
発行日
2024
出版物タイトル
Organic and Biomolecular Chemistry
22巻
9号
出版者
Royal Society of Chemistry (RSC)
開始ページ
1756
終了ページ
1764
ISSN
1477-0520
NCID
AA1168650X
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© The Royal Society of Chemistry 2024
論文のバージョン
author
PubMed ID
DOI
Web of Science KeyUT
関連URL
isVersionOf https://doi.org/10.1039/d3ob02089d
助成機関名
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