| ID | 67630 |
| Author |
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
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researchmap
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| Abstract | 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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| Note | 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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| Published Date | 2024
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| Publication Title |
Organic and Biomolecular Chemistry
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| Volume | volume22
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| Issue | issue36
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| Publisher | Royal Society of Chemistry (RSC)
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| Start Page | 7343
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| End Page | 7348
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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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| PubMed ID | |
| DOI | |
| Web of Science KeyUT | |
| Related Url | isVersionOf https://doi.org/10.1039/d4ob01218f
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| Funder Name |
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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