Synthesis of the elusive dibenzannelated dihydropyrene dibenzo[e,l]dimethyldihydropyrene, a molecular photo-switch
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. The synthesis of the first benzannelated -15,16-dihydropyrene: An example of the reduction of the diatropicity of a 14π-electron system by benzannelation
2. Benzannelated annulenes. II. The synthesis of trans-12b,12c-dimethyl-12b,12c- dihydrobenzo(e)pyrene. An indication of the exceptional aromaticity of the 15,16-dimethyldihydropyrene system
3. Benzannelated annulenes. 3. A clear demonstration of importance of symmetrical Kekule structures to diatropicity (aromaticity). Synthesis of a stable, highly diatropic, dibenzannulene
4. An Experimental Estimation of Aromaticity Relative to That of Benzene. The Synthesis and NMR Properties of a Series of Highly Annelated Dimethyldihydropyrenes: Bridged Benzannulenes
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