Issue 36, 2018

Synthesis of polycyclic spirooxindoles via an asymmetric catalytic one-pot stepwise Aldol/chloroetherification/aromatization procedure

Abstract

A general method for the synthesis of chiral pentacyclic spirooxindoles containing a tetrahydropyrano[2,3-b]indole scaffold through a one-pot stepwise sequence from 3-(3-indolomethyl)oxindole, paraformaldehyde and NCS is reported. Furthermore, the pentacyclic spirooxindoles could be transformed to bispirooxindole and other structurally diverse spirocyclic oxindoles.

Graphical abstract: Synthesis of polycyclic spirooxindoles via an asymmetric catalytic one-pot stepwise Aldol/chloroetherification/aromatization procedure

Supplementary files

Article information

Article type
Communication
Submitted
18 Jul 2018
Accepted
12 Aug 2018
First published
24 Aug 2018

Org. Biomol. Chem., 2018,16, 6647-6651

Synthesis of polycyclic spirooxindoles via an asymmetric catalytic one-pot stepwise Aldol/chloroetherification/aromatization procedure

Y. Jiang, S. Yu, Y. Yang, Y. Liu, X. Xu, X. Zhang and W. Yuan, Org. Biomol. Chem., 2018, 16, 6647 DOI: 10.1039/C8OB01713A

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