32595-98-5Relevant articles and documents
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Duus,Lawesson
, p. 387,398 (1971)
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Heteroannulation of 4-oxo-4H-1-benzopyrans (chromosomes) via the conjugate addition of haloalkanols in the presence of base
Cremins,Hayes,Wallace
, p. 9431 - 9438 (2007/10/02)
Chromones (4-oxo-4H-1-benzopyrans) bearing electron-withdrawing substituents at C-3 react with 2-haloethanols and potassium carbonate in acetone to produce tetrahydrofuro[2,3-b][1]benzopyran-4-ones, the heteroannulation proceeding via the conjugate addition of the haloethanol to the chromone, followed by intramolecular alkylation. Under the conditions of the reaction, the products derived from chromone-3-carbaldehydes undergo in situ deformylation.