| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5280257 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
A new, general route to the 1,2-diaryl-substituted pyrrolo[2,1-a]isoquinolines has been developed via the 1,5-dipolar electrocyclisation reactions of azomethine ylides derived from readily available stilbenic acid derivatives. This method was applied to the concise construction of a lamellarin skeleton.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![1,5-Electrocyclisation of azomethine ylides leading to pyrrolo[2,1-a]isoquinolines-concise construction of the lamellarin skeleton](/preview/png/5280257.png "First Page Preview: 1,5-Electrocyclisation of azomethine ylides leading to pyrrolo[2,1-a]isoquinolines-concise construction of the lamellarin skeleton")
Authors
Miklós Nyerges, László TÅke,