[3 + 2]-Cycloaddition of Nonstabilized Azomethine Ylides. 10. An Efficient Strategy for the Construction of x-Azatricyclo[m.n.0.0a,b]alkanes by Intramolecular Cycloaddition of Cyclic Azomethine Ylide

Pandey, Ganesh ; Sahoo, Akhila K. ; Bagul, Trusar D. (2000) [3 + 2]-Cycloaddition of Nonstabilized Azomethine Ylides. 10. An Efficient Strategy for the Construction of x-Azatricyclo[m.n.0.0a,b]alkanes by Intramolecular Cycloaddition of Cyclic Azomethine Ylide Organic Letters, 2 (15). pp. 2299-2301. ISSN 1523-7060

Full text not available from this repository.

Official URL: http://doi.org/10.1021/ol006070s

Related URL: http://dx.doi.org/10.1021/ol006070s

Abstract

Various new structural entities related to x-azatricyclo[m.n.0.0a,b]alkanes are constructed by the intramolecular [3 + 2] dipolar cycloaddition of nonstabilized cyclic azomethine ylides. The ylide is generated by the sequential double desilylation of N-alkyl α,α‘-bis(trimethylsilyl)cyclic amines using Ag(I)F as a one-electron oxidant.

Item Type:Article
Source:Copyright of this article belongs to American Chemical Society.
ID Code:122471
Deposited On:02 Aug 2021 18:59
Last Modified:02 Aug 2021 18:59

Repository Staff Only: item control page