A Novel Electrophilic Diamination Reaction of Alkenes

A three‐component electrophilic reaction transforms olefins into imidazoline and diamine derivatives (see scheme). Rhodium(II) heptafluorobutyrate dimer (2 mol %) was utilized as the catalyst and N,N‐dichloro‐p‐toluenesulfonamide (TsNCl2) and acetonitrile as the nitrogen sources. Modest to good yiel...

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Veröffentlicht in:Angewandte Chemie International Edition 2001-11, Vol.40 (22), p.4277-4280
Hauptverfasser: Li, Guigen, Wei, Han-Xun, Kim, Sun Hee, Carducci, Michael D.
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Sprache:eng
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Zusammenfassung:A three‐component electrophilic reaction transforms olefins into imidazoline and diamine derivatives (see scheme). Rhodium(II) heptafluorobutyrate dimer (2 mol %) was utilized as the catalyst and N,N‐dichloro‐p‐toluenesulfonamide (TsNCl2) and acetonitrile as the nitrogen sources. Modest to good yields (45–82 %) and high regio‐ and stereoselectivity were achieved.
ISSN:1433-7851
1521-3773
DOI:10.1002/1521-3773(20011119)40:22<4277::AID-ANIE4277>3.0.CO;2-I