Regioselective oxidation of indoles to 2-oxindoles
Author:
Affiliation:
1. Division of Organic Chemistry
2. National Chemical Laboratory (CSIR)
3. Pune 411 008
4. India
5. Academy of Scientific and Innovative Research (AcSIR)
Abstract
Facile regioselective oxidation of indoles to 2-oxindoles promoted by sulfuric acid adsorbed on silica gel is reported.
Funder
University Grants Commission
Science and Engineering Research Board
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2019/OB/C9OB00764D
Reference41 articles.
1. Modern Methods for Total Synthesis of Important Oxindole Alkaloids
2. Oxidative Fragmentations and Skeletal Rearrangements of Oxindole Derivatives
3. Synthesis of novel symmetrical 2-oxo-spiro[indole-3,4′-pyridines] by a reaction of oxindoles with 1,2-diaza-1,3-dienes
4. Design, Synthesis, and Evaluation of Indolinones as Triple Angiokinase Inhibitors and the Discovery of a Highly Specific 6-Methoxycarbonyl-Substituted Indolinone (BIBF 1120)
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