Literature DB >> 22148908

A bis(heptafulvenyl)-dicyanoethylene thermoswitch with two sites for ring closure.

Søren Lindbæk Broman1, Anne Ugleholdt Petersen, Christian Gregers Tortzen, Johan Vibenholt, Andrew D Bond, Mogens Brøndsted Nielsen.   

Abstract

Suitably functionalized vinylheptafulvenes (VHFs) act as thermoswitches undergoing ring closure to the corresponding dihydroazulenes (DHAs). Here we present the synthesis of a new such thermoswitch incorporating two heptafulvene rings on a dicyanoethylene unit. The synthetic protocol explores both the tropylium species as an electrophile and as a leaving group in the generation of the heptafulvene units. The thermally induced ring closure was enhanced as a result of two accessible sites for the reaction to occur.
© 2011 American Chemical Society

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Year:  2011        PMID: 22148908     DOI: 10.1021/ol2030586

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  1 in total

1.  Investigating the continuous synthesis of a nicotinonitrile precursor to nevirapine.

Authors:  Ashley R Longstreet; Suzanne M Opalka; Brian S Campbell; B Frank Gupton; D Tyler McQuade
Journal:  Beilstein J Org Chem       Date:  2013-11-20       Impact factor: 2.883

  1 in total

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