
Heterocycles p. 1803 - 1808 (1993)
Update date:2022-08-03
Topics:
Takao, Hisashi
Endo, Yoshinori
Horie, Tokunaru
The palladium-catalyzed coupling reaction of 3-benzyloxy-5-bromo-2-methyl-4H-pyran-4-one (2b) with phenylboronic acid afforded efficiently 3-benzyloxy-2-methyl-5-phenyl-4H-pyran-4-one (3b-1), and the benzyloxy group of the resultant product was cleaved by hydrolysis with conc. hydrochloric acid in acetic acid to give 5-phenyl-3-hydroxy-2-methyl-4H-pyran-4-one (4b-1) in high yield.This method was applicable as a general method for synthesizing 5-aryl-3-hydroxy-4H-pyran-4-ones (4) from the 5-bromo-4H-pyran-4-ones (1).
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Doi:10.1021/acschemneuro.9b00447
(2019)Doi:10.1007/BF00903115
(1973)Doi:10.1021/jo016325v
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(2019)Doi:10.1002/hlca.19430260331
(1943)