Literature DB >> 18802525

From dioxime oxalates to dihydropyrroles and phenanthridines via iminyl radicals.

Fernando Portela-Cubillo1, Eoin M Scanlan, Jackie S Scott, John C Walton.   

Abstract

Dioxime oxalates are useful precursors for the clean generation of iminyl radicals by sensitised UV photolysis and can be adapted for serviceable preparations of 3,4-dihydro-2H-pyrroles and phenanthridines.

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Year:  2008        PMID: 18802525     DOI: 10.1039/b808625g

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  1 in total

1.  The oxime portmanteau motif: released heteroradicals undergo incisive EPR interrogation and deliver diverse heterocycles.

Authors:  John C Walton
Journal:  Acc Chem Res       Date:  2014-03-21       Impact factor: 22.384

  1 in total

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