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<dc:creator>Netz, Natalie</dc:creator>
<dc:creator>Díez Poza, Carlos</dc:creator>
<dc:creator>Barbero Pérez, María Asunción</dc:creator>
<dc:creator>Opatz, Till</dc:creator>
<dc:date>2017</dc:date>
<dc:description>A modular synthesis of unsymmetrical BODIPY dyes&#xd;
based on a [6π] electrocyclization to construct both pyrrole&#xd;
rings is presented. The products carry four aryl moieties in positions&#xd;
1, 3, 5, and 7, which can be freely selected, as well as optional substitution in positions 2 and 8. The method employs acetophenones, benzaldehydes as well as glycine nitrile or&#xd;
glycine ethyl ester as the key building blocks.</dc:description>
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<dc:publisher>John Wiley &amp; Sons, Inc</dc:publisher>
<dc:title>Modular De novo Synthesis of Unsymmetrical BODIPY Dyes Possessing Four Different Aryl Substituents</dc:title>
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