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2-Alkyl-2,3-dihydro-y-pyrones

A synthesis of 2-alkyl-2,3-dihydro-y-pyrones (187) from methoxybutenyne and aldehydes has been described (83TL4551). The condensation of lithiomethoxy-butenyne (184) with aldehydes at -78°C leads to the secondary alcohols 185, which form the dihydropyrones 187 via hydration of the acetylenic bond and hydrolysis of the methoxyethenyl group to the ketoenol 186 (0°C, p-TSA, THF, H2O or 30% HCIO4, 20 min) folowed by intramolecular cycloaddition. [Pg.206]


See also in sourсe #XX -- [ Pg.82 , Pg.206 ]

See also in sourсe #XX -- [ Pg.82 , Pg.206 ]

See also in sourсe #XX -- [ Pg.82 , Pg.206 ]

See also in sourсe #XX -- [ Pg.82 , Pg.206 ]




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