Literature DB >> 16372103

Electrochemical annulation of five-membered rings through dearomatization of furans and thiophenes.

Jeffrey B Sperry1, Ion Ghiviriga, Dennis L Wright.   

Abstract

A new methodology for the annulation of five-membered carbocyclic rings onto enones through the dearomatizing electrochemical cyclization of furans and thiophenes has been developed.

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Year:  2005        PMID： 16372103     DOI： 10.1039/b513532j

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


  3 in total

1.  Synthetic Organic Electrochemical Methods Since 2000: On the Verge of a Renaissance.

Authors:  Ming Yan; Yu Kawamata; Phil S Baran
Journal:  Chem Rev       Date:  2017-10-09       Impact factor: 60.622

Review 2.  Synthetic Organic Electrochemistry: An Enabling and Innately Sustainable Method.

Authors:  Evan J Horn; Brandon R Rosen; Phil S Baran
Journal:  ACS Cent Sci       Date:  2016-05-05       Impact factor: 14.553

3.  The tandem ring opening/ring closing metathesis route to oxaspirocycles: an approach to phelligridin G.

Authors:  Harold D Cooper; Dennis L Wright
Journal:  Molecules       Date:  2013-02-21       Impact factor: 4.411
  3 in total

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