Iodine-Promoted N–H/α,β-C(sp 3 )‑Trifunctionalization of l‑Proline: Access to 3,4-Dihydrobenzo[ b ][1,7]naphthyridines via Consecutive Decarboxylation/RingOpening/Dicyclization
2019
A N–H/α,β-C(sp3)-trifunctionalization of l-proline, proceeding through an iodine-promoted consecutive decarboxylation/ring-opening/dicyclization process, is achieved. This strategy affords structurally diverse fused N-heterocycles in good yields with a wide substrate scope. Preliminary mechanistic studies indicate that catabolism of l-proline might be involved in this cascade reaction and the in situ generated intermediate 4-aminobutanal was identified as the key intermediate. Notably, this domino strategy enriches the reactivity of versatile l-proline in the synthesis of fused heterocycles.
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