Aromatische Spirane, 14. Mitt. Darstellung von 2,2′-Spirobi-( s-hydrindacen) und seinen Vorstufen.

Autor: Neudeck, Horst
Zdroj: Chemical Monthly / Monatshefte für Chemie; 1987, Vol. 118 Issue 5, p627-657, 31p
Abstrakt: The title compound 35 was prepared by catalytic reduction of the diones 29 a and 11a. 29 a was synthesized by systematic anellation of fivemembered rings to the positions 5,6 and 5′,6′, resp., of 2,2′-spirobiindane. The preparation of 11 a was achieved by Friedel-Crafts cyclisation of bis-(5-indanylmethyl)-malonic acid. s-Hydrindacene-1-one 5 a was prepared as a precursor for the synthesis of 11 a (see forthcoming publication) and its derivates as models for corresponding anellation and substitution reactions. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index