Literature DB >> 15228287

Purpurinimide-fullerene dyads: introduction of fullerene moiety at various peripheral positions of the purpurinimide system.

Guolin Li1, Mahabeer P Dobhal, Masayuki Shibata, Ravindra K Pandey.   

Abstract

[reaction: see text] Fullerene was regioselectively introduced at various peripheral positions of N-hexyl-purpurinimide for photoinduced electron transfer studies. Remarkably different effects of the position of the fullerene moiety in the formation of atropisomers were observed.

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Year:  2004        PMID: 15228287     DOI: 10.1021/ol0492290

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


  2 in total

1.  Rational routes to formyl-substituted chlorins.

Authors:  Chinnasamy Muthiah; Jayeeta Bhaumik; Jonathan S Lindsey
Journal:  J Org Chem       Date:  2007-06-22       Impact factor: 4.354

2.  Remarkable features of the McMurry reaction conditions in dimerization of formyl- and 2-formylvinylpurpurinimides. Electrochemistry of monomeric Ni(II) purpurinimide and the corresponding dyads.

Authors:  Lalit N Goswami; Manivannan Ethirajan; Mahabeer P Dobhal; Min Zhang; Joseph R Missert; Masayuki Shibata; Karl M Kadish; Ravindra K Pandey
Journal:  J Org Chem       Date:  2009-01-16       Impact factor: 4.354

  2 in total

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