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Abstract | Cited by

The phase-transfer catalyst promoted intramolecular transformation of pyrrole-2-carbaldehyde substituted Morita–Baylis–Hillman adducts has been disclosed, providing an efficient way to construct pyrrolo[1,2-a]azepin-7(6H)-one skeletons in moderate to good yields (up to 92%) under mild conditions.

Graphical abstract: A cascade reaction of pyrrole-2-carbaldehyde substituted Morita–Baylis–Hillman adducts in the presence of tetrabutylammonium hydroxide or acetate to construct aza-heterocycles

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