Benutzer: Gast  Login
Titel:

Electrophilic Cyclization of 1,6-Enynes

Dokumenttyp:
Journal Article
Autor(en):
Harschneck, T.; Kirsch, S. F.; Wegener, M.
Abstract:
The NIS-mediated iodocyclization of 1,6-enynes is described. While 1,6-enynes with a cation-stabilizing substituent at C2 position undergo 6-exo cyclization in poor yields, 1,6-enynes with donor substituents at C1 position favor the 5-exo mode of cyclization. The resulting five-membered carbocycles are obtained in moderate to good yields, thus demonstrating another facet in the iodocyclization of enynes.
Kongresstitel:
ISI Document Delivery No.: 758ZC Times Cited: 5 Cited Reference Count: 51 Harschneck, Tobias Kirsch, Stefan F. Wegener, Michael Deutsche Forschungsgemeinschaft (DFG); Fonds der Chemischen Industrie (FCI); TUM Graduate School This project was supported by the Deutsche Forschungsgemeinschaft (DFG), the Fonds der Chemischen Industrie (FCI), and the TUM Graduate School. 5 Georg thieme verlag kg Stuttgart
Zeitschriftentitel:
Synlett
Jahr:
2011
Heft / Issue:
8
Seitenangaben Beitrag:
1151-1153
Volltext / DOI:
doi:10.1055/s-0030-1259938
 BibTeX