Octaselenocyclododecane†
Dr. Guoxiong Hua
School of Chemistry, University of St Andrews, Fife, KY16 9ST (UK), Fax: (+44) 1334-463-834
Search for more papers by this authorDr. John M. Griffin
School of Chemistry, University of St Andrews, Fife, KY16 9ST (UK), Fax: (+44) 1334-463-834
Search for more papers by this authorDr. Sharon E. Ashbrook
School of Chemistry, University of St Andrews, Fife, KY16 9ST (UK), Fax: (+44) 1334-463-834
Search for more papers by this authorProf. Alexandra M. Z. Slawin
School of Chemistry, University of St Andrews, Fife, KY16 9ST (UK), Fax: (+44) 1334-463-834
Search for more papers by this authorCorresponding Author
Prof. J. Derek Woollins
School of Chemistry, University of St Andrews, Fife, KY16 9ST (UK), Fax: (+44) 1334-463-834
School of Chemistry, University of St Andrews, Fife, KY16 9ST (UK), Fax: (+44) 1334-463-834Search for more papers by this authorDr. Guoxiong Hua
School of Chemistry, University of St Andrews, Fife, KY16 9ST (UK), Fax: (+44) 1334-463-834
Search for more papers by this authorDr. John M. Griffin
School of Chemistry, University of St Andrews, Fife, KY16 9ST (UK), Fax: (+44) 1334-463-834
Search for more papers by this authorDr. Sharon E. Ashbrook
School of Chemistry, University of St Andrews, Fife, KY16 9ST (UK), Fax: (+44) 1334-463-834
Search for more papers by this authorProf. Alexandra M. Z. Slawin
School of Chemistry, University of St Andrews, Fife, KY16 9ST (UK), Fax: (+44) 1334-463-834
Search for more papers by this authorCorresponding Author
Prof. J. Derek Woollins
School of Chemistry, University of St Andrews, Fife, KY16 9ST (UK), Fax: (+44) 1334-463-834
School of Chemistry, University of St Andrews, Fife, KY16 9ST (UK), Fax: (+44) 1334-463-834Search for more papers by this authorWe are grateful to the University of St Andrews for support.
Graphical Abstract
Der erste seiner Art? Ein einfach aufgebauter, zwölfgliedriger C-Se-Heterocyclus (siehe Struktur; blau C, gelb Se, schwarz H) wurde bei der Umsetzung von sekundären Aminen mit dem Woollins-Reagens erhalten. Die Bildung des Rings verläuft über intermediäre Diselenoate und erfordert ein polares Lösungsmittel wie Dichlormethan.
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