A new and efficient method for the 'one-step' synthesis of (Z)-1,2-bis(benzodithienyl)ethenes has been set up using double Suzuki coupling between stereochemically defined diboronic acid esters and 2-iodo benzodithiophene. The new Z-alkenes thus obtained can be easily and efficiently photochemically cyclised to the newly substituted tetrathia[7]helicenes.
A novel and efficient approach to (Z)-1,2-bis(benzodithienyl)ethene precursors of tetrathia[7]helicenes
Baldoli C;Bossi A;
2005
Abstract
A new and efficient method for the 'one-step' synthesis of (Z)-1,2-bis(benzodithienyl)ethenes has been set up using double Suzuki coupling between stereochemically defined diboronic acid esters and 2-iodo benzodithiophene. The new Z-alkenes thus obtained can be easily and efficiently photochemically cyclised to the newly substituted tetrathia[7]helicenes.File in questo prodotto:
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Descrizione: A novel and efficient approach to (Z)-1,2-bis(benzodithienyl)ethene precursors of tetrathia[7]helicenes
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