Literature DB >> 17912409

Microwave-assisted preparations of dihydropyrroles from alkenone O-phenyl oximes.

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

Abstract

Microwave irradiation of alkenone O-phenyl oximes produces iminyl radicals that ring close to yield dihydropyrrole derivatives; pyrroles and pyridines can be obtained from related precursors.

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Year:  2007        PMID： 17912409     DOI： 10.1039/b712582h

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


  5 in total

Review 1.  Controlled microwave heating in modern organic synthesis: highlights from the 2004-2008 literature.

Authors:  C Oliver Kappe; Doris Dallinger
Journal:  Mol Divers       Date:  2009-04-21       Impact factor: 2.943

2.  Copper-catalyzed aerobic radical C-C bond cleavage of N-H ketimines.

Authors:  Ya Lin Tnay; Gim Yean Ang; Shunsuke Chiba
Journal:  Beilstein J Org Chem       Date:  2015-10-19       Impact factor: 2.883

3.  A new route to α-carbolines based on 6π-electrocyclization of indole-3-alkenyl oximes.

Authors:  Sophie J Markey; William Lewis; Christopher J Moody
Journal:  Org Lett       Date:  2013-11-26       Impact factor: 6.005

4.  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

5.  Dichotomous mechanistic behavior in Narasaka-Heck cyclizations: electron rich Pd-catalysts generate iminyl radicals.

Authors:  Nicholas J Race; Adele Faulkner; Megan H Shaw; John F Bower
Journal:  Chem Sci       Date:  2015-12-01       Impact factor: 9.825
  5 in total

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