| ID | 67630 |
| 著者 |
Tokushige, Keisuke
Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Kobori, Yuito
Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Asai, Shota
School of Pharmacy, Shujitsu University
Abe, Takumi
Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
ORCID
Kaken ID
researchmap
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| 抄録 | 2-Aminobenzoyl chlorides possess both a nucleophilic nitrogen atom and an electrophilic carbonyl group, and thus selective acylation of nucleophiles is challenging; self-dimerization and sluggish reactions occur. Herein, we introduce a new synthetic protocol using 2-aminobenzoyl surrogates, allowing concise entry to decorated 2-aminobenzoyl derivatives in the absence of transition metals, acid chlorides, and specific reagents.
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| 備考 | This is an Accepted Manuscript of an article published by Royal Society of Chemistry (RSC).
This fulltext file will be available in Aug. 2025.
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| 発行日 | 2024
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| 出版物タイトル |
Organic and Biomolecular Chemistry
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| 巻 | 22巻
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| 号 | 36号
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| 出版者 | Royal Society of Chemistry (RSC)
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| 開始ページ | 7343
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| 終了ページ | 7348
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| ISSN | 1477-0520
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| NCID | AA1168650X
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| 資料タイプ |
学術雑誌論文
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| 言語 |
英語
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| OAI-PMH Set |
岡山大学
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| 著作権者 | © The Royal Society of Chemistry 2024
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| 論文のバージョン | author
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| PubMed ID | |
| DOI | |
| Web of Science KeyUT | |
| 関連URL | isVersionOf https://doi.org/10.1039/d4ob01218f
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| 助成機関名 |
Japan Society for the Promotion of Science
Japan Science and Technology Agency
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| 助成番号 | 22K06503
JPMJSP2126
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