Add time:08/28/2019 Source:sciencedirect.com
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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