[3 + 2]-Cycloaddition of nonstabilized azomethine ylides. 10. An efficient strategy for the construction of x-azatricyclo[m.n.0.0 < sup > a,b < /sup > ]alkanes by intramolecular cycloaddition of cyclic azomethine ylide
[3 + 2]-Cycloaddition of nonstabilized azomethine ylides. 10. An efficient strategy for the construction of x-azatricyclo[m.n.0.0 < sup > a,b < /sup > ]alkanes by intramolecular cycloaddition of cyclic azomethine ylide
| dc.contributor.author | Pandey, Ganesh | |
| dc.contributor.author | Sahoo, Akhila K. | |
| dc.contributor.author | Bagul, Trusar D. | |
| dc.date.accessioned | 2022-03-27T08:36:04Z | |
| dc.date.available | 2022-03-27T08:36:04Z | |
| dc.date.issued | 2000-07-27 | |
| dc.description.abstract | (equation presented) 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. | |
| dc.identifier.citation | Organic Letters. v.2(15) | |
| dc.identifier.issn | 15237060 | |
| dc.identifier.uri | 10.1021/ol006070s | |
| dc.identifier.uri | https://pubs.acs.org/doi/10.1021/ol006070s | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/11137 | |
| dc.title | [3 + 2]-Cycloaddition of nonstabilized azomethine ylides. 10. An efficient strategy for the construction of x-azatricyclo[m.n.0.0 < sup > a,b < /sup > ]alkanes by intramolecular cycloaddition of cyclic azomethine ylide | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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