Metal-free base-mediated oxidative annulation cascades to 3-substituted-3-hydroxyoxindole and its 3-spirocyclic derivative
Author(s) -
Min Liu,
ChunXia Zhang,
Mingruo Ding,
Bencan Tang,
Fengzhi Zhang
Publication year - 2017
Publication title -
green chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.221
H-Index - 221
eISSN - 1463-9270
pISSN - 1463-9262
DOI - 10.1039/c7gc01783a
Subject(s) - annulation , chemistry , derivative (finance) , oxidative phosphorylation , metal , free base , base (topology) , stereochemistry , combinatorial chemistry , organic chemistry , mathematics , biochemistry , business , catalysis , mathematical analysis , finance , salt (chemistry)
A simple and efficient method was developed for the construction of the medicinally important 3-substituted-3-hydroxyoxindole and its 3-spirocyclic derivatives with readily available aniline derivatives as starting materials. This highly atom- and step-economical one-pot protocol was carried out under metal-free base-mediated conditions through a novel oxidative annulation strategy with oxygen as the oxidant. The key intermediates were isolated and confirmed. A reasonable reaction pathway was proposed and supported by the preliminary experiments, and the computational studies were carried out to understand the energetics of the key rearrangement reaction.
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