| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5273402 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
A one-pot approach to the synthesis of novel glycosylidene-based quinolines is described. The reaction involves a Lewis acid catalyzed Povarov addition followed by oxidation of the resulting spiroanellated tetrahydroquinoline intermediates to yield the open-ring glycosylidene-derived quinoline.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Peter H. Dobbelaar, Cecilia H. Marzabadi,