2-Hydroxyindoline-3-triethylammonium Bromide: A Reagent for Formal C3-Electrophilic Reactions of Indoles
Author:
Affiliation:
1. Faculty of Pharmaceutical Sciences, Health Sciences University of Hokkaido, Ishikari-tobetsu, Hokkaido 0610293, Japan
2. Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 0600812, Japan
Funder
Japan Society for the Promotion of Science
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b01940
Reference69 articles.
1. Indoles in Multicomponent Processes (MCPs)
2. Nucleophilic Substitution of Hydrogen in Heterocyclic Chemistry
3. Electrophilicity: the “dark-side” of indole chemistry
4. Lewis Acid and Fluoroalcohol Mediated Nucleophilic Addition to the C2 Position of Indoles
5. Synthesis of 3a-(Indol-3-yl)-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indole Core of Leptosins D-F Based on Nucleophilic Substitution Reaction on Indole Nucleus
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