このエントリーをはてなブックマークに追加
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
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.
Note
This is an Accepted Manuscript of an article published by American Chemical Society
Published Date
2016-04-27
Publication Title
Organic Letters
Volume
volume18
Issue
issue9
Publisher
American Chemical Society
Start Page
2020
End Page
2023
ISSN
1523-7060
NCID
AA11347843
Content Type
Journal Article
language
英語
OAI-PMH Set
岡山大学
Copyright Holders
https://creativecommons.org/licenses/by-nc-nd/4.0/deed.ja
File Version
author
PubMed ID
DOI
Web of Sience KeyUT
Related Url
https://doi.org/10.1021/acs.orglett.6b00629