2019
DOI: 10.1002/slct.201903811
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Synthesis of Benzo[1,2‐b:4,5‐b’]dithiophene and Benzocondensed Thiaheterocycles

Abstract: A two‐step synthesis of benzo[1,2‐b:4,5‐b’]dithiophene (BDT) was carried out starting from 3‐thiophene carbaldehyde as the sole thiophene precursor. This method involves the selective lithiation of the 2‐position of 3‐thiophenecarbaldehyde ethylene acetal, followed by the condensation with 3‐thiophenecarbaldehyde and subsequent dehydrative cycloaromatization of the dithienylmethanol intermediate to give BDT. This synthetic pathway was extended to other thiophene benzocondensed heterocycles.

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Cited by 2 publications
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“…The thienannulation reaction shows a more innovative way to construct BDT. More recently, BDT units have been constructed by 3-thiophenecarboxaldehyde ( Figure 2 ) [ 17 ]. As shown in Figure 2 , the intermediate benzo[1,2-b:4,5- b′]dithiophene-4,8-dione played an important role in the synthesis of a BDT unit with various lateral substitutions to tune the properties of BDT-based molecules.…”
Section: Synthesis and Developments Of Bdt-based Donor Molecules In Oscsmentioning
confidence: 99%
“…The thienannulation reaction shows a more innovative way to construct BDT. More recently, BDT units have been constructed by 3-thiophenecarboxaldehyde ( Figure 2 ) [ 17 ]. As shown in Figure 2 , the intermediate benzo[1,2-b:4,5- b′]dithiophene-4,8-dione played an important role in the synthesis of a BDT unit with various lateral substitutions to tune the properties of BDT-based molecules.…”
Section: Synthesis and Developments Of Bdt-based Donor Molecules In Oscsmentioning
confidence: 99%