Issue 14, 2021

Base-enabled access to diastereoselective spirofuran oxindoles and γ-functionalized allenoates

Abstract

Base assisted divergent reactivity of isatins and allenoates has been achieved, which afforded diastereoselective spirofuran oxindoles and γ-functionalized allenoates. The DBU mediated Morita–Baylis–Hillman (MBH) reaction followed by the cascade annulation through the stabilized β-ammonium enolate intermediate led to the spiro-framework, wherein DABCO furnished the γ-functionalized allenoates. The protocol offers access to biologically relevant functionalized oxindole scaffolds with an excellent substrate scope under mild reaction conditions.

Graphical abstract: Base-enabled access to diastereoselective spirofuran oxindoles and γ-functionalized allenoates

Supplementary files

Article information

Article type
Communication
Submitted
24 Nov 2020
Accepted
12 Jan 2021
First published
12 Jan 2021

Chem. Commun., 2021,57, 1746-1749

Base-enabled access to diastereoselective spirofuran oxindoles and γ-functionalized allenoates

B. D., A. K. M. S., J. Krishnan, A. C. S., A. R. R., E. Suresh and S. B. Somappa, Chem. Commun., 2021, 57, 1746 DOI: 10.1039/D0CC07715A

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