Symmetry 2010, 2(2), 950-969; doi:10.3390/sym2020950
Review

Synthesis and Reactions of Dibenzo[a,e]pentalenes

Received: 28 January 2010; in revised form: 11 March 2010 / Accepted: 20 April 2010 / Published: 21 April 2010
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: Pentalene has recently received a considerable amount of attention as a ligand in sandwich-type transition metal complexes. In contrast, dibenzo[a,e]pentalene (hereafter denoted as dibenzopentalene), which is more π-extended than pentalene, has received less attention, despite its potential usefulness as a building block of ladder-type π-conjugated molecules, which have recently received growing interest. However, very recently, several novel efficient methods for the synthesis of dibenzopentalenes have been reported. This review surveys recent advances in the synthesis and reactions of dibenzopentalenes and describes the aromaticity of their ionic species.
Keywords: dibenzopentalene; thermolysis; skeletal rearrangement; reductive cyclization; catalyst; redox reaction
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MDPI and ACS Style

Saito, M. Synthesis and Reactions of Dibenzo[a,e]pentalenes. Symmetry 2010, 2, 950-969.

AMA Style

Saito M. Synthesis and Reactions of Dibenzo[a,e]pentalenes. Symmetry. 2010; 2(2):950-969.

Chicago/Turabian Style

Saito, Masaichi. 2010. "Synthesis and Reactions of Dibenzo[a,e]pentalenes." Symmetry 2, no. 2: 950-969.

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