The synthesis and characterization of 1-formyl-2-acylcyclopentadienylthallium compounds
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文摘
The reaction of sodium cyclopentadienide with RCOOEt (R=Me, Ph, 2-thienyl, or OEt) or Bup>tp>COCl followed by Vilsmeier reagent in the presence of excess sodium methoxide produces the 2-substituted-6-dimethylaminofulvenes 1ae in modest yields. Basic hydrolysis results in the formation of 2-substituted-6-hydroxyfulvenes 2ae in very good yields. Subsequent deprotonation with TlOEt yields the 1-formyl-2-acyl or carboethoxy cyclopentadienylthallium compounds 3ae.

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