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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 11, 1981 - Issue 11
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Original Articles

An Improved Synthesis of 2,2-Dialkyl-1,3-Indanediones

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Pages 913-915 | Published online: 05 Dec 2006

References

  • Dolbier , W. R. Jr. , Matsui , K. , Mc Cullagh , L. and Anapolle , K. E. 1979 . J. Org. Chem. , 44 : 2842
  • Aebi , A. , Gyurech‐Vado , E. , Hofstetter , E. and Waser , P. 1963 . Pharm. Acta Helv. , 38 : 407
  • Ando , T. and Yamawaki , J. 1979 . Chem. Lett. , : 45 and 755
  • In no case monoalkylation products were formed even when less than 2 equivalents of alkylating agent was used. In contrast it has been reported (3) that in the same conditions an aliphatic substrate (2,4‐pentanedione) gives rise to a mixture of mono C‐ and O‐ alkylation products
  • Mosher , W. A. and Soeder , R. W. 1971 . J. Org. Chem. , 36 : 1561 2‐Methyl‐1,3‐indanedione Ib was prepared according to

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