The reaction of 4-X-5-alkylthio-3H-1,2-dithiole-3-thione (1) with Fischer carbene complexes (2) gives, as a main product, cyclohexa dithiine derivatives due to insertion of the carbene ligand into the C3 C4 bond of the heterocycle. The reaction takes place with 1 where the alkyl substituents in posi
✦ LIBER ✦
Insertion of NH into the rheniumcarbon bonds of a Fischer-type rhenacyclobutadiene. Preparation and characterization of azarhenacyclic complexes
✍ Scribed by Véronique Plantevin; Judith C. Gallucci; Andrew Wojcicki
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 743 KB
- Volume
- 222
- Category
- Article
- ISSN
- 0020-1693
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