1,6ak 4 -Dithia-6-azapentalenes (7a)-( 7h), (12a), and (12b) have been synthesized by the reaction of 5-aryl-3-benzylidene-3H-1,2-dithioles with isonitriles in the presence of phosphoryl chloride and by the reaction of 3-benzyl-and 3-methyl-1k 4 , 2-dithiol-1-ylium salts with isonitriles. Possible m
Synthesis of 1λ4,2-diselenol-1-ylium salts
✍ Scribed by David H. Reid; Beate G. Rose; Michael G. Jackson
- Book ID
- 102846565
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 568 KB
- Volume
- 4
- Category
- Article
- ISSN
- 1042-7163
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✦ Synopsis
Abstract
Seven bis‐(1λ^4^,2‐diselenol‐1‐ylium) tetrachloroferrates have been prepared by reaction of 1,3‐diketones or 1,3‐ketoaldehydes with hydrogen selenide and iron(III) chloride in ethanol saturated with hydrogen chloride. They decompose gradually in air. The corresponding 1λ^4^,2‐diselenol‐1‐ylium perchlorates have been prepared by reaction of the tetrachloroferrates with perchloric acid in acetic acid and are stable. The tetrachloroferrates react with benzenediazonium tetrafluoroborate to give 6,6aλ^4^‐diselena‐1,2‐diazapentalenes.
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