Asymmetric Intramolecular [3 + 2] Cycloaddition Reactions of Acylhydrazones/Olefins Using a Chiral Zirconium Catalyst
Catalytic asymmetric intramolecular [3 + 2] cycloaddition of hydrazone/olefins has been attained. In the presence of a chiral zirconium catalyst prepared from zirconium alkoxide and a BINOL derivative, the desired pyrazolidine derivatives were obtained in high yields with high selectivities. The pro...
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Veröffentlicht in: | Journal of the American Chemical Society 2002-11, Vol.124 (46), p.13678-13679 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Catalytic asymmetric intramolecular [3 + 2] cycloaddition of hydrazone/olefins has been attained. In the presence of a chiral zirconium catalyst prepared from zirconium alkoxide and a BINOL derivative, the desired pyrazolidine derivatives were obtained in high yields with high selectivities. The products were easily converted to 1,3-diamine or β-aminonitrile derivatives by N−N bond cleavage. |
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ISSN: | 0002-7863 1520-5126 |
DOI: | 10.1021/ja027681d |