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Metallocenes 2-alkyl-4-aryl-substituted

Synthetic Approaches Toward 2-Alkyl-4-Aryl-Substituted ansa Metallocenes... [Pg.267]

Indanones are very useful and versatile intermediates in the synthesis of metallocene catalysts. Scheme 1 has the synthetic scheme originally used for the preparation of 2-alkyl-4-aryl-substituted ansa metallocenes [9-11]. In the first part of this sequence, the biaryl unit is assembled and the missing carbon atoms are introduced as a side chain. The reaction of 2-phenylbenzyl bromide with malonic acid ethyl ester under basic conditions, followed by a decarboxylation, affords the 2-(2-phenylbenzyl)propionic acid. Chlorination and Friedel-Crafts acylation yields the 2-methyl-4-phenylindanone in 93 % yield. From here, only a few standard transformations are required to complete the synthesis, finally yielding the desired metallocene. [Pg.267]


See other pages where Metallocenes 2-alkyl-4-aryl-substituted is mentioned: [Pg.212]    [Pg.699]    [Pg.704]    [Pg.23]    [Pg.871]    [Pg.944]    [Pg.109]    [Pg.79]    [Pg.9]    [Pg.564]    [Pg.269]    [Pg.155]    [Pg.198]    [Pg.951]    [Pg.5]    [Pg.11]    [Pg.4561]    [Pg.18]    [Pg.210]    [Pg.341]   


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2-Substituted alkyl 3-

Alkyl substitute

Alkylated metallocenes

Aryl substituted

Aryl-substitution

Substitution alkylation

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