The cycloaddition of hex-3-yn-2,5-dione onto a rc-CS2 Iron complex 3 and on 3-thioxo-1.2dithioles affords diietylated intermediates which can be readily converted into di or tetraacetylated derivatives of the 1,3-dithiole (5,6) and tetrathiafulvalene (2.8) series, some represemative electrochemical
β¦ LIBER β¦
Chemistry of geminal-dithiolates derived from cyano-substituted tetrathiafulvalenes
β Scribed by Edward M. Engler; Vishnu V. Patel; Robert R. Schumaker
- Book ID
- 104244385
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 188 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
Tetracyanotetrathiafulvalene reacts with two equivalents of thiol salts (RS-) to give 1,2-dicyano-1,2-di RS ethene and a geminal dithiolate intermediate which reacts with a variety of reagents to provide novel tetrathioethene derivatives, such as reaction with 3-chloro-2-butanone and acid to give dimethyldicyanotetrathiafulvalene.
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