Issue 88, 2024

Synthesis of dispiro-orthoester via an acetal oxo-carbenium ion

Abstract

The first dispiro orthoester via a spiroacetal oxo-carbenium ion is presented. Oxidative dearomatization of phloretic esters results in a bifunctional electrophilic spiroacetal oxo-carbenium ion, which undergoes a double nucleophilic addition by diol delivering a range of unusual dispiro-orthoesters with an excellent diversity.

Graphical abstract: Synthesis of dispiro-orthoester via an acetal oxo-carbenium ion

Supplementary files

Article information

Article type
Communication
Submitted
24 Jun 2024
Accepted
28 Aug 2024
First published
02 Sep 2024

Chem. Commun., 2024,60, 12860-12863

Synthesis of dispiro-orthoester via an acetal oxo-carbenium ion

M. Kumar, S. Singh and P. Subramanian, Chem. Commun., 2024, 60, 12860 DOI: 10.1039/D4CC03031A

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