Literature DB >> 32323682

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.

Vladimir E Zhulanov1, Valeria A Vigovskaya1, Maksim V Dmitriev1, Pavel S Silaichev1, Andrey N Maslivets1, Michael Rubin2.   

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.

Entities:  

Year:  2020        PMID: 32323682     DOI: 10.1039/d0ob00451k

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  Cycloaddition of Huisgen 1,4-dipoles: synthesis and rapid epimerization of functionalized spiropyrido[2,1-b][1,3]oxazine-pyrroles and related products.

Authors:  Andrew R Galeev; Anna A Moroz; Maksim V Dmitriev; Andrey N Maslivets
Journal:  RSC Adv       Date:  2021-12-22       Impact factor: 3.361

  1 in total

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