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1,3-Dipolar Cycloaddition of Nitrones with Electron-rich Alkenes Catalyzed by Yb(OTf)3

✍ Scribed by Chang-Tao Qian; Long-Cheng Wang; Rui-Fang Chen


Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
456 KB
Volume
19
Category
Article
ISSN
0256-7660

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✦ Synopsis


Abstract

1,3‐Dipolar cycloaddition of nitrones with ethyl vinyl ether or 2,3‐dihydrofuran proceeds smoothly in the presence of a catalytic amount (10 mol%) of ytterbium triflate to afford isoxazolidines and dicyclic isoxazolidine respectively with good yields and high stereoselectivity.


πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Yb(OTf)3-Catalyzed
✍ S. MINAKATA; T. EZOE; K. NAKAMURA; I. RYU; M. KOMATSU πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 33 KB πŸ‘ 1 views

The ytterbium triflate catalyzed 1,3-dipolar cycloaddition of diphenylnitrone (I) with the crotylamides (II) is investigated. The diastereoselectivity is found to depend on the nature of the amide auxiliary and the solvent.