Issue 30, 2021, Issue in Progress

A formal intermolecular [4 + 1] cycloaddition reaction of 3-chlorooxindole and o-quinone methides: a facile synthesis of spirocyclic oxindole scaffolds

Abstract

Herein, we developed an efficient and straightforward method for the rapid synthesis of spirocyclic oxindole scaffolds via the [4 + 1] cyclization reaction of 3-chlorooxindole with o-quinone methides (o-QMs), which were generated under mild conditions. The products could be obtained in excellent yields with numerous types of 3-chlorooxindole. This methodology features mild reaction conditions, high atom-economy and broad substrate scope.

Graphical abstract: A formal intermolecular [4 + 1] cycloaddition reaction of 3-chlorooxindole and o-quinone methides: a facile synthesis of spirocyclic oxindole scaffolds

Supplementary files

Article information

Article type
Paper
Submitted
09 Feb 2021
Accepted
08 May 2021
First published
24 May 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 18576-18579

A formal intermolecular [4 + 1] cycloaddition reaction of 3-chlorooxindole and o-quinone methides: a facile synthesis of spirocyclic oxindole scaffolds

C. Lin, Q. Xing and H. Xie, RSC Adv., 2021, 11, 18576 DOI: 10.1039/D1RA01086G

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