Access to 3,4-furan dithiolate: towards 3,4-dialkylsulfanylfurans and their Diels–Alder adducts with acrylonitrile
✍ Scribed by Pierre Frère; Nuria Gallego-Planas; Philippe Blanchard; Gilles Mabon; David Rondeau
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 155 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
The convenient synthesis of symmetrical and unsymmetrical 3,4-dialkylsulfanylfurans from 3,4-furandithiolate is described. The reactivity of the furan cycle as a diene in Diels-Alder reactions with acrylonitrile is discussed in relation to the presence of one or two thiolato substituents.
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a,a'-dibromo ketonesin thepresenceof iron powder,or a-ehloro ketones in the prxence of frietftylantine,have been shown to MU very essify with fnranor cyclopentsdiene when water was usedas solvent. 631997Publishedby Elsevier Science Ltd.