| ID | 55376 |
| FullText URL | |
| Author |
Morimoto, Naoki
Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Div Pharmaceut Sci
Morioku, Kumika
Okayama Univ, Fac Engn, Dept Appl Chem & Biotechnol
Suzuki, Hideyuki
Okayama Univ, Res Core Interdisciplinary Sci
Takeuchi, Yasuo
Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Div Pharmaceut Sci
Nishina, Yuta
Okayama Univ, Res Core Interdisciplinary Sci
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| Abstract | Indole readily undergoes nucleophilic substitution at the C3 site, and many indole derivatives have been functionalized using this property. Indole also forms indolium, which allows electrophilic addition in acidic conditions, but current examples have been limited to intramolecular reactions. C2 site-selective nucleophilic addition to indole derivatives using fluoroalcohol and a Lewis acid was developed.
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| Note | This is an Accepted Manuscript of an article published by American Chemical Society
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| Published Date | 2016-04-27
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| Publication Title |
Organic Letters
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| Volume | volume18
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| Issue | issue9
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| Publisher | American Chemical Society
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| Start Page | 2020
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| End Page | 2023
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| ISSN | 1523-7060
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| NCID | AA11347843
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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 | https://creativecommons.org/licenses/by-nc-nd/4.0/deed.ja
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| File Version | author
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| PubMed ID | |
| DOI | |
| Web of Science KeyUT | |
| Related Url | https://doi.org/10.1021/acs.orglett.6b00629
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