The First Tetrathio‐Substituted Cyclobutane‐1,2,3,4‐tetracarbonitrile — A New Highly Substituted Cyclobutane
Anke Spannenberg, Hans‐Jürgen Holdt, Joachim Teller, Klaüs Praefcke, Jürgen Kopf
Abstract
Anke Spannenberg, Hans‐Jürgen Holdt, Joachim Teller, Klaüs Praefcke, Jürgen Kopf
Abstract
Abstract The first tetrathio‐substituted cyclobutane‐1,2,3,4‐tetracarbonitrile 9 was obtained by an intramolecular photoinduced [2 + 2] cycloaddition reaction of the 14‐membered macrocyclic tetrathioether 7 containing two 1,2‐dicyano‐1,2‐dithioethene units in dichloromethane in 73% yield.
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Abstract The first tetrathio‐substituted cyclobutane‐1,2,3,4‐tetracarbonitrile 9 was obtained by an intramolecular photoinduced [2 + 2] cycloaddition reaction of the 14‐membered macrocyclic tetrathioether 7 containing two 1,2‐dicyano‐1,2‐dithioethene units in dichloromethane in 73% yield.
Key concepts: Cyclobutane, Chemistry, Dichloromethane, Cycloaddition, Intramolecular force, Yield (engineering), Photochemistry, Medicinal chemistry