We studied the influence of acetic acid concentration on the deamination and dephosphonylation of the adduct resulting of the nucleophilic reaction between adequate ot-metalated phosphonate and immlnium salt. to enhance the yield of such reactions in order to access efficiently a lot of unsymmetrica
Synthesis of unsymmetrically substituted TTF derivatives via the “phosphonate way”. Some investigations on the scope of the method
✍ Scribed by H.J. Cristau; F. Darviche; M.-T. Babonneau; J.-M. Fabre; E. Torreilles
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 482 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0040-4020
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✦ Synopsis
The scope and limitations of the .synthesis of tmsymmetricaily substituted TIT derivatives via the "'phosphonate way" was investigated using as precursors 1.3-dithiol-2-yl-phosphonates and 1.3-dithiol-2-yliden iminium salts with various substituents on the dithiole cycles. Except for the un-or monosubstituted phosphonates, the one-pot procedure proves to be general and affords in all cases a significant improvement in the overall yields in TIT derivatives. The study has shown also that the formation of the intermediate adducts occurs in high yield, but their transformation into TIT derivatives, in presence of anhydrous acetic acid, is strongly sensitive to the nature of the various substituents, particularly on the iminium part
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An improved synthesis of unsymmetrical tetrathiafulvalenes (TTFs) (5 a-c, 5 f-g, 7) is presented which results in higher yields of unsymmetrical TTFs when compared to existing methods. The synthetic method consists of pre-equilibration of thiones containing electron withdrawing groups with P(OEt)3 a