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2256479 
Journal Article 
Modern Friedel-Crafts chemistry. Part 31. An efficient synthetic approach to mono-, di- and triphenylindane derivatives via direct Friedel-Crafts cyclialkylation of selected phenylated alkanols 
Khalaf, AliA; El-Khawaga, AM; Awad, IM; Abd El-Aal, HAK 
2009 
314-323 
Facile procedures for the synthesis of mono-, di- and triphenylindanee derivatives from the alcohols 1-4 are described thus treatment with 85% H(2)SO(4), AlCl(3)/CH(3)NO(2), H(3)PO(4) and/or PPA under varying conditions produced 1,1-dimethyl-3-phenylindanee 6 from 2-methyl-4,4-diphenyl-2- butanol 1, 3,3-dimethyl-1,1-diphenylindanee 9 from 2-methyl-4,4,4-triphenyl-2-butanol 2, 1-methyl- 1,3-diphenylindanee 12 from 2,4,4-triphenyl-2-butanol 3 and 1,1,3-triphenylindanee 15 from 1,1,3,3-tetraphenyl-1-propanol 4. The starting and final products were characterized by elemental, IR, (1)H NMR and MS analyses. 
Friedel-Crafts cyclialkylation; 1,1-dimethyl-3-phenylindane; 3,3-dimethyl-1,1-diphenylindane; 1-methyl-1,3-diphenylindane; 1,1,3-triphenylindane; di-; tri- and tetraphenyl alkanols