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Ring-opening reaction of 2,5-dioctyldithieno[2,3-b:3',2'-d]thiophene in the presence of aryllithium reagents
- Source :
- Beilstein Journal of Organic Chemistry, Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 767-774 (2013)
- Publication Year :
- 2013
- Publisher :
- Beilstein-Institut, 2013.
-
Abstract
- In this paper, the ring-opening reaction of 2,5-dioctyldithieno[2,3-b:3',2'-d]thiophene with aryllithium in THF at low temperature to generate 2'-arylthio-3,3'-bithiophene-2-carbaldehydes is studied. Nine examples are explored and all the products are characterized by 1H NMR, 13C NMR and HRMS. The relative relationship between the structures of aryl groups and the efficiency of ring-opening reactions are discussed.
- Subjects :
- aryllithium reagents
Stereochemistry
Aryl
Organic Chemistry
nucleophilicity
2'-arylthio-3,3'-bithiophene-2-carbaldehyde
Carbon-13 NMR
Ring (chemistry)
Medicinal chemistry
Full Research Paper
lcsh:QD241-441
chemistry.chemical_compound
Chemistry
chemistry
Nucleophile
lcsh:Organic chemistry
Reagent
Thiophene
Proton NMR
lcsh:Q
dithieno[2,3-b:3',2'-d]thiophene
lcsh:Science
ring-opening reaction
Subjects
Details
- Language :
- English
- ISSN :
- 18605397
- Volume :
- 9
- Database :
- OpenAIRE
- Journal :
- Beilstein Journal of Organic Chemistry
- Accession number :
- edsair.doi.dedup.....2c981f3b5f277bbb6b891246df502ea7