| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278507 | Tetrahedron Letters | 2009 | 5 Pages |
Abstract
Palladium-catalyzed cyclization/cyclopropanation can be used to convert a range of substituted cyclic N-aryl allyl/methallyl amines efficiently and selectively to the corresponding fused tetrahydropyridine/cyclopropane-fused isoquinoline derivatives via β-hydrogen elimination or a domino sequence.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Sukla Nandi, Jayanta K. Ray,