Issue 17, 2020

Dipyrazolodioxadiazocines as shelf-stable “ready-to-use” precursors for an in situ generation of enolate-iminium 1,4-dipoles: a straightforward atom-economical approach to pyrazolo[5,1-d][1,3,5]dioxazines

Abstract

An original, facile and highly efficient method for the in situ generation of cyclic enolate-iminium 1,4-dipoles via unique thermal decomposition of easily available dipyrazolodioxadiazocines has been developed. Various substituted pyrazolo[5,1-d][1,3,5]dioxazines have been prepared in high yields via unusual cycloconversion of dipyrazolodioxadiazocines in the presence of ketones. Furthermore, the developed method is 100% atom economical and proceeds under metal-, catalyst- and solvent-free conditions.

Graphical abstract: Dipyrazolodioxadiazocines as shelf-stable “ready-to-use” precursors for an in situ generation of enolate-iminium 1,4-dipoles: a straightforward atom-economical approach to pyrazolo[5,1-d][1,3,5]dioxazines

Supplementary files

Article information

Article type
Paper
Submitted
02 Mar 2020
Accepted
17 Apr 2020
First published
20 Apr 2020

Org. Biomol. Chem., 2020,18, 3382-3391

Dipyrazolodioxadiazocines as shelf-stable “ready-to-use” precursors for an in situ generation of enolate-iminium 1,4-dipoles: a straightforward atom-economical approach to pyrazolo[5,1-d][1,3,5]dioxazines

V. E. Zhulanov, V. A. Vigovskaya, M. V. Dmitriev, P. S. Silaichev, A. N. Maslivets and M. Rubin, Org. Biomol. Chem., 2020, 18, 3382 DOI: 10.1039/D0OB00451K

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