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 monos
Mechanistic investigations of the formation of TTF derivatives via the phosphonate way
β Scribed by H-J Cristau; F. Darviche; E. Torreilles; J-M Fabre
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 211 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
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 unsymmetrical TTF derivatives. A mechanism is proposed for the formation of TIT, including steps, i~ to i-. The potential concurrent formation of phosphonate 1 and other b)-products is also discussed.
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