Data di Pubblicazione:
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.
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
benzannulation · benzodithiophene · cycloaromatization · fused-ring systems · sulfur heterocycles
Elenco autori:
Baldoli, Clara
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