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Synthesis of Benzo[1,2-b:4,5-b']dithiophene and Benzocondensed Thiaheterocycles

Academic Article
Publication Date:
2019
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.
Iris type:
01.01 Articolo in rivista
Keywords:
benzannulation · benzodithiophene · cycloaromatization · fused-ring systems · sulfur heterocycles
List of contributors:
Baldoli, Clara
Handle:
https://iris.cnr.it/handle/20.500.14243/362292
Published in:
CHEMISTRYSELECT
Journal
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http://www.scopus.com/record/display.url?eid=2-s2.0-85075617871&origin=inward
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