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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 7, 1977 - Issue 4
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Original Articles

The Preparation and Reactions of Anions of Certain Schiff Bases

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Pages 261-268 | Received 03 Mar 1977, Published online: 23 Oct 2006

References

  • To whom inquiries should be addressed.
  • Beam , C. F. , Dyer , M. C. D. , Schwarz , R. A. and Hauser , C. R. 1970 . J. Org. Chem. , 35 : 1806
  • Foote , R. S. , Beam , C. F. and Hauser , C. R. 1970 . J. Heterocycl. Chem. , 7 : 589
  • Beam , C. F. , Foote , R. S. and Hauser , C. R. 1971 . J. Chem. Soc., C , : 1658
  • Sandifer , R. M. , Davis , S. E. and Beam , C. F. 1976 . Synth. Comm. , 6 : 339
  • Sandifer , R. M. , Dasher , L. W. , Hollinger , W. M. , Thomas , C. W. , Reames , D. C. , Beam , C. F. , Foote , R. S. and Hauser , C. R. 1975 . J. Heterocycl. Chem. , 12 : 1159
  • Beam , C. F. , Reames , D. C. , Harris , C. E. , Dasher , L. W. , Hollinger , W. M. , Shealy , N. L. , Sandifer , R. M. , Perkins , M. and Hauser , C. R. 1975 . J. Org. Chem. , 40 : 514
  • Reames , D. C. , Harris , C. E. , Dasher , L. W. , Sandifer , R. M. , Hollinger , W. M. and Beam , C. F. 1975 . J. Heterocycl. Chem. , 12 : 779
  • Park , C. A. , Beam , C. F. , Kaiser , E. M. , Kaufman , R. J. , Henoch , F. E. and Hauser , C. R. 1976 . J. Heterocycl. Chem. , 13 : 449
  • Griffiths , J. S. , Beam , C. F. and Hauser , C. R. 1971 . J. Chem. Soc., C , : 974
  • Beam , C. F. , Foote , R. S. and Hauser , C. R. 1972 . J. Heterocycl. Chem. , 9 : 183
  • Henoch , F. E. and Hauser , C. R. 1969 . Can. J. Chem. , 47 : 157
  • Henoch , F. E. , Hampton , K. G. and Hauser , C. R. 1969 . J. Am. Chem. , 91 : 676
  • Kaiser , E. M. , Henoch , F. E. and Hauser , C. R. 1968 . J. Am. Chem. Soc. , 90 : 7287
  • The C(α)-H resonance for the starting material for IIa was noted at δ 2.00 ppm. The imine for preparation of II b-e, had a C(α)-H resonance at α 2.23 ppm.
  • Light , R. J. and Hauser , C. R. 1961 . J. Org. Chem. , 26 : 1716
  • We have successfully found the appropriate conditions for the di-Aldol condensation of 1,6-azine dicarbanions. The completed project will be reported in another journal. See also: reference 13.
  • The same product was ottained when one, two or three molar equivalents of base were used per molar equivalent of imine. The best yields were obtained by the procedure described.
  • An nmr spectrum of the same material was taken on a Varian Associates A-60 NMR Spectrometer (Univ. of S. C. at Columbia). The sharp singlet of δ 1.83 ppm (CDC13) supported the assignment of this absorption to C(α)-hydrogens.

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