γ-lodothioethers as a source of sulfurcontaining radicals: Reaction with electrophilic olefins

Anales de Quimica

Volumn 92, Issue 5, 1996, Pages 280-284

  Foubelo, Francisco ^a   Gutiérrez, Ana Maria ^a  

^a UNIVERSITY OF ALICANTE   (Spain)

Author keywords

Electrophilic olefins; Functionalised radical; Lodothioethers

Indexed keywords

EID: 0040296092     PISSN: 11302283     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (25)

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10. This type of compounds can he stabilised by transforming the heteroatom functionality into an anionic moiety. See, for instance: Bachki A. Foubelo F. Vus M (1995) Tetrahedron:Asymmetry 6:2081-2092
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14. This methodology has been also applied to the preparation of enolic (10a). homoenolic [10b] and acrylic [10c] radicals, which can he considered or y-functionalised radicals:
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