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
Hauptverfasser: Kobayashi, Shū, Shimizu, Haruka, Yamashita, Yasuhiro, Ishitani, Haruro, Kobayashi, Jun
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Sprache:eng
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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.
ISSN:0002-7863
1520-5126
DOI:10.1021/ja027681d