Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5281342 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
The cycloalkeno[1,2-d]furo[2,3-b]pyridine skeleton was conveniently synthesized from fused 4-(2-cyanovinyloxy)butanenitriles in one step through sequential intramolecular Michael addition, β-elimination and intramolecular nucleophilic addition. This sequence thus consists of a novel Truce-Smiles type rearrangement followed by cyclization. The 5-amino derivatives were transformed further to lactams in good yields.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Kensuke Okuda, Norimasa Watanabe, Takashi Hirota, Kenji Sasaki,