Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5270705 | Tetrahedron Letters | 2014 | 5 Pages |
Abstract
A cascade of inverse electron demand Diels–Alder reaction of 6-aminocoumarin-derived aldimines with an excess of styrene and oxidative aromatization of the formal Povarov adducts under autotandem iodine catalysis in aqueous micellar conditions provides direct access to a small library of substituted pyridine annulated coumarins in good to acceptable yields (12 examples). The unusual formation of linearly annulated pyridocoumarins under essentially neutral conditions is a remarkable feature of the protocol.
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