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  • Synthesis of [60]fullerene-fused tetrahydronaphthalene and indane derivatives via a pathway switched by aluminum chloride.

Synthesis of [60]fullerene-fused tetrahydronaphthalene and indane derivatives via a pathway switched by aluminum chloride.

Organic letters (2011-10-29)
Tong-Xin Liu, Fa-Bao Li, Guan-Wu Wang
ZUSAMMENFASSUNG

The addition of aluminum chloride to the manganese acetate-mediated radical reaction of [60]fullerene with 2-arylmalonates, 2-benzylmalonates, and 2-arylcyanoacetates can switch the reaction pathway and affords a variety of structurally novel and scarce [60]fullerene-fused tetrahydronaphthalene and indane derivatives. These products are formed probably through radical addition, followed by Friedel-Crafts-type annulation.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Indan, 95%
Supelco
Indan, analytical standard