Synthesis of thiophene-based building blocks via facile α-monoiodination

Synlett

Volumn , Issue 5, 2001, Pages 634-636

  Boas, Ulrik ^a   Dhanabalan, Anantharaman ^a   Greve, Daniel R ^a   Meijer, E W ^a  

^a EINDHOVEN UNIVERSITY OF TECHNOLOGY   (Netherlands)

Author keywords

Monoiodination; N iodosuccinimide; Oligothiophenes; Thiophene based segments

Indexed keywords

THIOPHENE DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; IODINATION; SYNTHESIS;

EID: 0035038377     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2001-13361     Document Type: Article

References (17)

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12. 3): 374.27. Found: 374.0; GC: 99% purity
13. 2): 292.15. Found: 291.9; GC: 95% purity
14. 2): 371.14. Found: 371.6; GC: 98% purity
15. 3); 341.4. Found: 342.0; GC; 96% purity
16. 2): 298.5. Found: 298.0; GC: 97% purity
17. Compounds 2 and 3 were prepared by Stille reaction between 2-(tributyl-stannyl)-thiophene and 1.4-dibromo-benzene or 4.7-dibromo-benzo[2.1.3]thiadiazole, respectively, according to: Dhanabalan, A.; Boas, U.; van Duren, J. K. J.; Janssen, R. A, J.; To be published.