Efficient Synthesis of Benzo Fused Tetrathiahelicenes
journal contributionposted on 21.10.2011 by Deepali Waghray, Wienand Nulens, Wim Dehaen
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An efficient route toward the synthesis of symmetrical and unsymmetrical benzo fused tetrathiahelicenes substituted with electron donor (ED) and electron acceptor (EA) groups is reported. A common, readily available precursor 1,2- bis-(2-thienyl)benzene was used to synthesize different helicenes through a Wittig reaction, Stille coupling, and modified oxidative photocyclization.