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
|
巻 | 22巻
|
号 | 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
|